6-31668702-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668702
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668702
    reference: chr 6
allele count: 4
allele frequency: 3.381462820816285e-5
allele num: 118292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-315+17C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.*78+17C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.*78+17C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.48+17C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*296+17C>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*170+17C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.343+17C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.244+17C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.*78+17C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.*78+17C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*170+17C>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

6-31668721-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668721
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668721
    reference: chr 6
allele count: 1
allele frequency: 8.348639171814994e-6
allele num: 119780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.46G>A
  hgvsp: ENSP00000442151.1:p.Glu16Lys
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*294G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.242G>A
  hgvsp: ENSP00000410347.2:p.Arg81Gln
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.*76G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-317G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*168G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*168G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.*76G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.*76G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.341G>A
  hgvsp: ENSP00000379282.3:p.Arg114Gln
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.*76G>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg114Gln
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-31668725-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668725
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668725
    reference: chr 6
allele count: 1
allele frequency: 8.330278897737497e-6
allele num: 120044
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.*72C>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*164C>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.42C>G
  hgvsp: ENST00000538874.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-321C>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*164C>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.238C>G
  hgvsp: ENSP00000410347.2:p.Leu80Val
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.*72C>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.337C>G
  hgvsp: ENSP00000379282.3:p.Leu113Val
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.*72C>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.*72C>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*290C>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu113Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

6-31668727-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668727
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668727
    reference: chr 6
allele count: 1
allele frequency: 8.327365388138501e-6
allele num: 120086
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.236G>A
  hgvsp: ENSP00000410347.2:p.Cys79Tyr
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.*70G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.*70G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.*70G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*162G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*162G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-323G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.335G>A
  hgvsp: ENSP00000379282.3:p.Cys112Tyr
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.40G>A
  hgvsp: ENSP00000442151.1:p.Ala14Thr
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*288G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.*70G>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5828
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys112Tyr
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

6-31668739-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668739
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668739
    reference: chr 6
allele count: 1
allele frequency: 8.307165761185599e-6
allele num: 120378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.28C>T
  hgvsp: ENSP00000442151.1:p.Gln10Ter
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-335C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.*58C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*276C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.224C>T
  hgvsp: ENSP00000410347.2:p.Ala75Val
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.*58C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.323C>T
  hgvsp: ENSP00000379282.3:p.Ala108Val
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*150C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.*58C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*150C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.*58C>T
  variant of: http://identifiers.org/hgnc/13921
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln10Ter
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD

6-31668747-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668747
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668747
    reference: chr 6
allele count: 4
allele frequency: 3.320108235528479e-5
allele num: 120478
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.216A>G
  hgvsp: ENST00000440843.2:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.20A>G
  hgvsp: ENSP00000442151.1:p.Tyr7Cys
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*142A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.*50A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.*50A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*142A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.*50A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-343A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.*50A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*268A>G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.315A>G
  hgvsp: ENST00000395952.3:c.315A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5844
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr7Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-31668749-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668749
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668749
    reference: chr 6
allele count: 1
allele frequency: 8.298066550493736e-6
allele num: 120510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.*48C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.18C>T
  hgvsp: ENST00000538874.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*140C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-345C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*140C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.214C>T
  hgvsp: ENST00000440843.2:c.214C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.*48C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.313C>T
  hgvsp: ENST00000395952.3:c.313C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.*48C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.*48C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*266C>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu105Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

6-31668755-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668755
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668755
    reference: chr 6
allele count: 4
allele frequency: 3.319612269286947e-5
allele num: 120496
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*260T>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.*42T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.208T>C
  hgvsp: ENST00000440843.2:c.208T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*134T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*134T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-351T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.*42T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.307T>C
  hgvsp: ENST00000395952.3:c.307T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.12T>C
  hgvsp: ENST00000538874.1:c.12T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.*42T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.*42T>C
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu103Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

6-31668766-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668766
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668766
    reference: chr 6
allele count: 1
allele frequency: 8.300270588821196e-6
allele num: 120478
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*249A>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*123A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.197A>C
  hgvsp: ENSP00000410347.2:p.Tyr66Ser
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*123A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.*31A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-362A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.296A>C
  hgvsp: ENSP00000379282.3:p.Tyr99Ser
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.1A>C
  hgvsp: ENSP00000442151.1:p.Met1?
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.*31A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.*31A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.*31A>C
  variant of: http://identifiers.org/hgnc/13921
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

6-31668796-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668796
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668796
    reference: chr 6
allele count: 1
allele frequency: 8.398138972403716e-6
allele num: 119074
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.*1G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.*1G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.266G>A
  hgvsp: ENSP00000379282.3:p.Ser89Asn
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.*1G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.*1G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*93G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-30G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.167G>A
  hgvsp: ENSP00000410347.2:p.Ser56Asn
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-392G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*93G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*219G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser89Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-31668800-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668800
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668800
    reference: chr 6
allele count: 1
allele frequency: 8.411843876177658e-6
allele num: 118880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.195T>C
  hgvsp: ENST00000482224.1:c.195T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.163T>C
  hgvsp: ENST00000440843.2:c.163T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.138T>C
  hgvsp: ENST00000477462.1:c.138T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.195T>C
  hgvsp: ENST00000495769.1:c.195T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-396T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*215T>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*89T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.138T>C
  hgvsp: ENST00000498420.1:c.138T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*89T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.262T>C
  hgvsp: ENST00000395952.3:c.262T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-34T>C
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu88Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

6-31668802-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668802
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668802
    reference: chr 6
allele count: 4
allele frequency: 3.369272237196766e-5
allele num: 118720
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.260A>G
  hgvsp: ENSP00000379282.3:p.Tyr87Cys
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*87A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-36A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.161A>G
  hgvsp: ENSP00000410347.2:p.Tyr54Cys
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*87A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.193A>G
  hgvsp: ENSP00000419742.1:p.Thr65Ala
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.136A>G
  hgvsp: ENSP00000418331.1:p.Thr46Ala
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-398A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.136A>G
  hgvsp: ENSP00000420628.1:p.Thr46Ala
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.193A>G
  hgvsp: ENSP00000418170.1:p.Thr65Ala
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*213A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr87Cys
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

6-31668807-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668807
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668807
    reference: chr 6
allele count: 1
allele frequency: 8.462671157524161e-6
allele num: 118166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-2A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-2A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-2A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-2A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-2A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-2A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-2A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-2A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-2A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-2A>G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-2A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000266776
  ensembl transcript: ENST00000580775
  gene symbol: MIR4646
  hgvsc: ENST00000580775.1:n.62A>G
  variant of: http://identifiers.org/hgnc/41543
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*210-2A>G
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

6-31668814-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668814
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668814
    reference: chr 6
allele count: 2
allele frequency: 1.707796089146956e-5
allele num: 117110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-9C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000266776
  ensembl transcript: ENST00000580775
  gene symbol: MIR4646
  hgvsc: ENST00000580775.1:n.55C>T
  variant of: http://identifiers.org/hgnc/41543
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-9C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-9C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-9C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-9C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-9C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-9C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-9C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-9C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-9C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-9C>T
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-31668817-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668817
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668817
    reference: chr 6
allele count: 1
allele frequency: 8.615490652192642e-6
allele num: 116070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-12C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-12C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-12C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-12C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-12C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-12C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-12C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-12C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-12C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-12C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-12C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000266776
  ensembl transcript: ENST00000580775
  gene symbol: MIR4646
  hgvsc: ENST00000580775.1:n.52C>T
  variant of: http://identifiers.org/hgnc/41543
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

6-31668821-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668821
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668821
    reference: chr 6
allele count: 2
allele frequency: 1.750332563187006e-5
allele num: 114264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-16C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-16C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-16C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-16C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-16C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-16C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-16C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-16C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-16C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-16C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-16C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000266776
  ensembl transcript: ENST00000580775
  gene symbol: MIR4646
  hgvsc: ENST00000580775.1:n.48C>T
  variant of: http://identifiers.org/hgnc/41543
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

6-31668840-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668840
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668840
    reference: chr 6
allele count: 4
allele frequency: 3.874467260751646e-5
allele num: 103240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-35G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-35G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-35G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-35G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-35G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-35G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-35G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-35G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000266776
  ensembl transcript: ENST00000580775
  gene symbol: MIR4646
  hgvsc: ENST00000580775.1:n.29G>A
  variant of: http://identifiers.org/hgnc/41543
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-35G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-35G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-35G>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11315
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4749
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16393
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

6-31668841-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668841
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668841
    reference: chr 6
allele count: 4
allele frequency: 3.901601607459862e-5
allele num: 102522
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-36C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000266776
  ensembl transcript: ENST00000580775
  gene symbol: MIR4646
  hgvsc: ENST00000580775.1:n.28C>T
  variant of: http://identifiers.org/hgnc/41543
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-36C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-36C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-36C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-36C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-36C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-36C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-36C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-36C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-36C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-36C>T
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11479
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12902
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-31668855-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668855
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668855
    reference: chr 6
allele count: 1
allele frequency: 1.070274204251129e-5
allele num: 93434
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-50G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-50G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-50G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-50G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-50G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-50G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-50G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: mature_miRNA_variant
  ensembl gene: ENSG00000266776
  ensembl transcript: ENST00000580775
  gene symbol: MIR4646
  hgvsc: ENST00000580775.1:n.14G>A
  variant of: http://identifiers.org/hgnc/41543
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-50G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-50G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-50G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-50G>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: mature miRNA
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11846
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

6-31668857-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668857
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668857
    reference: chr 6
allele count: 7
allele frequency: 7.541803137390105e-5
allele num: 92816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-52G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-52G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-52G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: mature_miRNA_variant
  ensembl gene: ENSG00000266776
  ensembl transcript: ENST00000580775
  gene symbol: MIR4646
  hgvsc: ENST00000580775.1:n.12G>A
  variant of: http://identifiers.org/hgnc/41543
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-52G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-52G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-52G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-52G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-52G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-52G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-52G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-52G>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: mature miRNA
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17740
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8387
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

6-31668861-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668861
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668861
    reference: chr 6
allele count: 199
allele frequency: 2.193272494819909e-3
allele num: 90732
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-56A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-56A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-56A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: mature_miRNA_variant
  ensembl gene: ENSG00000266776
  ensembl transcript: ENST00000580775
  gene symbol: MIR4646
  hgvsc: ENST00000580775.1:n.8A>G
  variant of: http://identifiers.org/hgnc/41543
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-56A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-56A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-56A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-56A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-56A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-56A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-56A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-56A>G
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: mature miRNA
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12767
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18622
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 1.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9009
  bin: 2.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7429
  bin: 2.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 3.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 2
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

6-31668885-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668885
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668885
    reference: chr 6
allele count: 1
allele frequency: 1.286074386542518e-5
allele num: 77756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-80G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-80G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-80G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-80G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-80G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-80G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-80G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-80G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-80G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-80G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-80G>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4948
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6813
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

6-31668898-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668898
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668898
    reference: chr 6
allele count: 2
allele frequency: 2.760295903720879e-5
allele num: 72456
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-93C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-93C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-93C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-93C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-93C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-93C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-93C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-93C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-93C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-93C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-93C>T
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5651
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8076
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18390
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

6-31668898-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668898
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668898
    reference: chr 6
allele count: 1
allele frequency: 1.380147951860439e-5
allele num: 72456
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-93C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-93C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-93C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-93C>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-93C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-93C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-93C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-93C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-93C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-93C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-93C>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8076
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5651
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18390
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/6-31668905-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668905
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668905
    reference: chr 6
allele count: 68
allele frequency: 9.885157726413722e-4
allele num: 68790
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-100T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-100T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-100T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-100T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-100T>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-100T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-100T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-100T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-100T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-100T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-100T>G
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 2.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8544
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17812
  bin: 1.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 17930
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

6-31668906-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668906
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668906
    reference: chr 6
allele count: 1
allele frequency: 1.395011439093801e-5
allele num: 71684
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-101G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-101G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-101G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-101G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-101G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-101G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-101G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-101G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-101G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-101G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-101G>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5461
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8664
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17956
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17676
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

6-31668910-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668910
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668910
    reference: chr 6
allele count: 2
allele frequency: 2.789711543826369e-5
allele num: 71692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-105G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-105G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-105G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-105G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-105G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-105G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-105G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-105G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-105G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-105G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-105G>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17487
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18347
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8417
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

6-31668916-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668916
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668916
    reference: chr 6
allele count: 1
allele frequency: 1.401384567953138e-5
allele num: 71358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-111G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-111G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-111G>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-111G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-111G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-111G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-111G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-111G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-111G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-111G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-111G>C
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17335
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18637
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-31668918-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31668918
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31668918
    reference: chr 6
allele count: 2
allele frequency: 2.809856978279806e-5
allele num: 71178
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*210-113T>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-113T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*84-113T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*84-113T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-113T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-113T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-113T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.257-113T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-401-113T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-113T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-113T>G
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8041
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4934
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

6-31669007-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669007
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669007
    reference: chr 6
allele count: 1
allele frequency: 8.326117364950376e-6
allele num: 120104
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.256+44T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-402+44T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*83+44T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-202T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*83+44T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-202T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-202T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*209+44T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-202T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-202T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-202T>C
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/6-31669009-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669009
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669009
    reference: chr 6
allele count: 1
allele frequency: 8.327920185212944e-6
allele num: 120078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-402+42G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-204G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-204G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*83+42G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-204G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-204G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*83+42G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-204G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*209+42G>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-204G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.256+42G>T
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17237
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-31669013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669013
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669013
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 120208
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*209+38G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-208G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-208G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-208G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-208G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*83+38G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-208G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*83+38G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-402+38G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.256+38G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-208G>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 14963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-31669018-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669018
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669018
    reference: chr 6
allele count: 1
allele frequency: 8.30923654734603e-6
allele num: 120348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-213A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-213A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-213A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*209+33A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-213A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-402+33A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*83+33A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*83+33A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-213A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.256+33A>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-213A>C
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-31669024-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669024
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669024
    reference: chr 6
allele count: 4
allele frequency: 3.321321221581945e-5
allele num: 120434
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-219G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-219G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.256+27G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-402+27G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*83+27G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*83+27G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-219G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-219G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-219G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-219G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*209+27G>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

6-31669025-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669025
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669025
    reference: chr 6
allele count: 1
allele frequency: 8.301097405076952e-6
allele num: 120466
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*209+26G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*83+26G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-220G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-220G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-220G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-220G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-220G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*83+26G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-220G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-402+26G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.256+26G>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12557
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

6-31669029-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669029
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669029
    reference: chr 6
allele count: 1
allele frequency: 8.292148993333113e-6
allele num: 120596
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-224G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-224G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.256+22G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-224G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*83+22G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*209+22G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-224G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*83+22G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-402+22G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-224G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-224G>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

6-31669035-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669035
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669035
    reference: chr 6
allele count: 107
allele frequency: 8.862457965444696e-4
allele num: 120734
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*83+16A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*83+16A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-230A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-230A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-230A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-230A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-230A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*209+16A>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.256+16A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-402+16A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-230A>G
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 18930
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16909
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12721
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ

6-31669048-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669048
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669048
    reference: chr 6
allele count: 1
allele frequency: 8.273214640280627e-6
allele num: 120872
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-243C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-243C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-243C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*83+3C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*83+3C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-402+3C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-243C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*209+3C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-243C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-243C>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.256+3C>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.256+3C>A
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/6-31669056-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669056
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669056
    reference: chr 6
allele count: 2
allele frequency: 1.653849334325643e-5
allele num: 120930
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*78G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-251G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*204G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-251G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-407G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.251G>T
  hgvsp: ENSP00000379282.3:p.Arg84Met
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-251G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-251G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*78G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-251G>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-251G>T
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg84Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-31669068-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669068
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669068
    reference: chr 6
allele count: 1
allele frequency: 8.267879288962381e-6
allele num: 120950
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-263T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*66T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-263T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.239T>G
  hgvsp: ENSP00000379282.3:p.Phe80Cys
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-263T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*66T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*192T>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-419T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-263T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-263T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-263T>G
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe80Cys
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

6-31669071-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669071
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669071
    reference: chr 6
allele count: 2
allele frequency: 1.653493832468005e-5
allele num: 120956
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-266T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*189T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-266T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*63T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-266T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-266T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-422T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.236T>C
  hgvsp: ENSP00000379282.3:p.Phe79Ser
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-266T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*63T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-266T>C
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19608
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Phe79Ser
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/6-31669071-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669071
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669071
    reference: chr 6
allele count: 1
allele frequency: 8.267469162340024e-6
allele num: 120956
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-266T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-266T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-266T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-266T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.236T>G
  hgvsp: ENSP00000379282.3:p.Phe79Cys
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*189T>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*63T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-266T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*63T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-266T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-422T>G
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5067
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe79Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-31669072-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669072
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669072
    reference: chr 6
allele count: 2
allele frequency: 1.653685237551884e-5
allele num: 120942
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*62T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-267T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*188T>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-267T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-267T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-267T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.235T>G
  hgvsp: ENSP00000379282.3:p.Phe79Val
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-267T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-423T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-267T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*62T>G
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19611
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe79Val
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

6-31669075-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669075
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669075
    reference: chr 6
allele count: 2
allele frequency: 1.653958750268768e-5
allele num: 120922
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-426G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-270G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-270G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-270G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*59G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-270G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.232G>A
  hgvsp: ENSP00000379282.3:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*59G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*185G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-270G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-270G>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala78Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

6-31669076-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669076
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669076
    reference: chr 6
allele count: 1
allele frequency: 8.270204108637402e-6
allele num: 120916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-427C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-271C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*58C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*184C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-271C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-271C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*58C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.231C>T
  hgvsp: ENST00000395952.3:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-271C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-271C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-271C>T
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe77Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

http://identifiers.org/exac.variant/6-31669139-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669139
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669139
    reference: chr 6
allele count: 1
allele frequency: 8.640801866413203e-6
allele num: 115730
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-334T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*17-22T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*17-22T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-334T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-334T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-334T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-468-22T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-334T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*143-22T>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-334T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.190-22T>G
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7878
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11781
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ

6-31669149-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669149
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669149
    reference: chr 6
allele count: 1
allele frequency: 1.146499736305061e-5
allele num: 87222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*17-32A>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-344A>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-344A>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-344A>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*143-32A>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*17-32A>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.190-32A>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-344A>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-344A>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-468-32A>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-344A>T
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8483
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15896
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

6-31669149-T-TAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669149
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669151
    reference: chr 6
allele count: 679
allele frequency: 7.784733209511362e-3
allele num: 87222
alternate allele: TAC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*143-34_*143-33dupGT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*17-34_*17-33dupGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-346_-39-345dupGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-346_190-345dupGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-468-34_-468-33dupGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-346_133-345dupGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.190-34_190-33dupGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-346_190-345dupGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*17-34_*17-33dupGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-346_133-345dupGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-346_158-345dupGT
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16130
  bin: 1.25e1
  variant carriers: 329
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15896
  bin: 1.75e1
  variant carriers: 248
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6959
  bin: 7.5e0
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8483
  bin: 2.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 2.75e1
  variant carriers: 34
genotype quality: GenotypeQuality
num of homozygotes: 11
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

6-31669149-T-TACAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669149
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669153
    reference: chr 6
allele count: 1
allele frequency: 1.146499736305061e-5
allele num: 87222
alternate allele: TACAC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*143-36_*143-33dupGTGT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-348_190-345dupGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-348_133-345dupGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.190-36_190-33dupGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-468-36_-468-33dupGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-348_-39-345dupGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*17-36_*17-33dupGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-348_158-345dupGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*17-36_*17-33dupGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-348_133-345dupGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-348_190-345dupGTGT
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16130
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15896
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum

6-31669149-TAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669149
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669147
    reference: chr 6
allele count: 34761
allele frequency: 3.985347733370022e-1
allele num: 87222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*17-34_*17-33delGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*143-34_*143-33delGT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-346_133-345delGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.190-34_190-33delGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-346_190-345delGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*17-34_*17-33delGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-346_133-345delGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-346_-39-345delGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-468-34_-468-33delGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-346_158-345delGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-346_190-345delGT
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 167
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.25e1
  variant carriers: 998
genotype depth: GenotypeDepth
  all individuals: 6959
  bin: 7.5e0
  variant carriers: 5146
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 249
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 2.5e0
  variant carriers: 336
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.75e1
  variant carriers: 452
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 15896
  bin: 1.75e1
  variant carriers: 9556
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 2.75e1
  variant carriers: 2253
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 16130
  bin: 1.25e1
  variant carriers: 11026
genotype depth: GenotypeDepth
  all individuals: 8483
  bin: 2.25e1
  variant carriers: 5122
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
num of homozygotes: 5659
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: TAC
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ

6-31669149-TACAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669149
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669145
    reference: chr 6
allele count: 268
allele frequency: 3.072619293297562e-3
allele num: 87222
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.190-36_190-33delGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-468-36_-468-33delGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*17-36_*17-33delGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-348_190-345delGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*143-36_*143-33delGTGT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-348_-39-345delGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*17-36_*17-33delGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-348_133-345delGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-348_133-345delGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-348_190-345delGTGT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-348_158-345delGTGT
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8483
  bin: 2.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16130
  bin: 1.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 15896
  bin: 1.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6959
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 2.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: TACAC
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

6-31669152-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669152
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669152
    reference: chr 6
allele count: 1
allele frequency: 3.447324875896305e-5
allele num: 29008
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-347T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*17-35T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*143-35T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-347T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.190-35T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-347T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-347T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-468-35T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-347T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-347T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*17-35T>C
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8069
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

6-31669162-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669162
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669162
    reference: chr 6
allele count: 1
allele frequency: 9.807382997920834e-6
allele num: 101964
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*17-45T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-357T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.190-45T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-468-45T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-357T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-357T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*143-45T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-357T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-357T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*17-45T>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-357T>C
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15787
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/6-31669163-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669163
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669162
    reference: chr 6
allele count: 5
allele frequency: 4.927856185445084e-5
allele num: 101464
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-468-47delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*143-47delT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-359delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*17-47delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-359delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-359delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.190-47delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-359delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-359delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-359delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*17-47delT
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15825
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6027
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6151
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14398
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10090
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: CA
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/6-31669165-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669165
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669164
    reference: chr 6
allele count: 5
allele frequency: 4.815749426925818e-5
allele num: 103826
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-361delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-361delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-361delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-361delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-361delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-468-49delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-361delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*17-49delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*143-49delT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.190-49delT
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*17-49delT
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 14342
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16203
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10349
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: CA
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-31669166-A-ACC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669166
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669168
    reference: chr 6
allele count: 395
allele frequency: 5.327614577432495e-3
allele num: 74142
alternate allele: ACC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-363_-39-362dupGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.190-51_190-50dupGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*17-51_*17-50dupGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-468-51_-468-50dupGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-363_190-362dupGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-363_190-362dupGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-363_158-362dupGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-363_133-362dupGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*143-51_*143-50dupGG
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*17-51_*17-50dupGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-363_133-362dupGG
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 14238
  bin: 1.25e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10369
  bin: 2.25e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 3.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5075
  bin: 7.5e0
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 15917
  bin: 1.75e1
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5856
  bin: 2.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/6-31669166-A-ACCCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669166
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669170
    reference: chr 6
allele count: 3
allele frequency: 4.046289552480375e-5
allele num: 74142
alternate allele: ACCCC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*17-50_*17-49insGGGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-362_190-361insGGGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*17-50_*17-49insGGGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.190-50_190-49insGGGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-362_133-361insGGGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*143-50_*143-49insGGGG
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-362_190-361insGGGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-362_158-361insGGGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-468-50_-468-49insGGGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-362_133-361insGGGG
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-362_-39-361insGGGG
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5075
  bin: 7.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10369
  bin: 2.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 14238
  bin: 1.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 15917
  bin: 1.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5856
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/6-31669166-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669166
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669166
    reference: chr 6
allele count: 378
allele frequency: 5.098324836125273e-3
allele num: 74142
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-361T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-361T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-361T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*17-49T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-468-49T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-361T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*143-49T>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*17-49T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-361T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-361T>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.190-49T>G
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 3.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 2.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 5075
  bin: 7.5e0
  variant carriers: 181
genotype depth: GenotypeDepth
  all individuals: 10369
  bin: 2.25e1
  variant carriers: 152
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14238
  bin: 1.25e1
  variant carriers: 271
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5856
  bin: 2.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15917
  bin: 1.75e1
  variant carriers: 228
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 3.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

6-31669167-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669167
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669167
    reference: chr 6
allele count: 1
allele frequency: 9.601167501968239e-6
allele num: 104154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-39-362G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.190-362G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.158-362G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.190-362G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*17-50G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-468-50G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*17-50G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.190-50G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-362G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*143-50G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-362G>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15661
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

6-31669810-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669810
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669810
    reference: chr 6
allele count: 1
allele frequency: 8.578094976667581e-6
allele num: 116576
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.189+41C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.157+579C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-469+41C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*142+41C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-1005C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*16+41C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-1005C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-40+41C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*16+41C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.189+41C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.189+41C>T
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum

6-31669812-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669812
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669812
    reference: chr 6
allele count: 5
allele frequency: 4.289121073309657e-5
allele num: 116574
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-469+39G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-1007G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.157+577G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*16+39G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*16+39G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-1007G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*142+39G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.189+39G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-40+39G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.189+39G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.189+39G>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25536
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

6-31669816-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669816
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669816
    reference: chr 6
allele count: 1
allele frequency: 8.577359202648689e-6
allele num: 116586
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*142+35T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.157+573T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-1011T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*16+35T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.189+35T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.189+35T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-1011T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*16+35T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.189+35T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-469+35T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-40+35T>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

6-31669820-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669820
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669820
    reference: chr 6
allele count: 1
allele frequency: 8.577800651912849e-6
allele num: 116580
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-40+31A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*16+31A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*16+31A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.189+31A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-469+31A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-1015A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*142+31A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.157+569A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-1015A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.189+31A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.189+31A>G
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15507
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

6-31669828-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669828
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669828
    reference: chr 6
allele count: 3
allele frequency: 2.572942932125766e-5
allele num: 116598
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.189+23G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*16+23G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*16+23G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*142+23G>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-1023G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-469+23G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-1023G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.189+23G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.157+561G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-40+23G>C
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.189+23G>C
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

6-31669840-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669840
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669840
    reference: chr 6
allele count: 1
allele frequency: 8.575888033205839e-6
allele num: 116606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-1035C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*142+11C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.189+11C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*16+11C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-1035C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-469+11C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-40+11C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.157+549C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.189+11C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*16+11C>T
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.189+11C>T
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

6-31669847-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669847
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669847
    reference: chr 6
allele count: 1
allele frequency: 8.576182226719954e-6
allele num: 116602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-1042T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.189+4T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*16+4T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.189+4T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*142+4T>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-40+4T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*16+4T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-1042T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-469+4T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.157+542T>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.189+4T>A
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*142+4T>A
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

6-31669848-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669848
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669848
    reference: chr 6
allele count: 1
allele frequency: 8.576035127439883e-6
allele num: 116604
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-40+3A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.157+541A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*16+3A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.189+3A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-469+3A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*142+3A>G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*16+3A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.189+3A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-1043A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.189+3A>G
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-1043A>G
  variant of: http://identifiers.org/hgnc/13921
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*142+3A>G
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

6-31669857-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31669857
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31669857
    reference: chr 6
allele count: 1
allele frequency: 8.576623554838932e-6
allele num: 116596
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420585
  ensembl transcript: ENST00000492084
  gene symbol: ABHD16A
  hgvsc: ENST00000492084.1:c.*10G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000417566
  ensembl transcript: ENST00000468037
  gene symbol: ABHD16A
  hgvsc: ENST00000468037.1:c.*10G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000365002
  ensembl transcript: ENST00000375842
  gene symbol: ABHD16A
  hgvsc: ENST00000375842.4:c.-475G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418331
  ensembl transcript: ENST00000477462
  gene symbol: ABHD16A
  hgvsc: ENST00000477462.1:c.133-1052G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000379282
  ensembl transcript: ENST00000395952
  gene symbol: ABHD16A
  hgvsc: ENST00000395952.3:c.183G>A
  hgvsp: ENST00000395952.3:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000418170
  ensembl transcript: ENST00000495769
  gene symbol: ABHD16A
  hgvsc: ENST00000495769.1:c.183G>A
  hgvsp: ENST00000495769.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000442151
  ensembl transcript: ENST00000538874
  gene symbol: ABHD16A
  hgvsc: ENST00000538874.1:c.-46G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000419742
  ensembl transcript: ENST00000482224
  gene symbol: ABHD16A
  hgvsc: ENST00000482224.1:c.183G>A
  hgvsp: ENST00000482224.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000420628
  ensembl transcript: ENST00000498420
  gene symbol: ABHD16A
  hgvsc: ENST00000498420.1:c.133-1052G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204427
  ensembl protein: ENSP00000410347
  ensembl transcript: ENST00000440843
  gene symbol: ABHD16A
  hgvsc: ENST00000440843.2:c.157+532G>A
  variant of: http://identifiers.org/hgnc/13921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204422
  ensembl protein: ENSP00000475702
  ensembl transcript: ENST00000461287
  gene symbol: XXbac-BPG32J3.20
  hgvsc: ENST00000461287.1:c.*136G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu61Leu
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 1362
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6490
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 479
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1523
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 605
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 332
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45047
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 160
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.127075546841493e-5
allele num: 65284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9686
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11220
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16106
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.105e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.11e0

MQRankSum
type: SiteQuality
SIO_000300: 3.71e-1

DP
type: SiteQuality
SIO_000300: 1.546445e6

QD
type: SiteQuality
SIO_000300: 1.195e1

GenotypeDepth
all individuals: 29
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 669
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 71
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 854
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46808
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1378
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6614
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 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: 9904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.751969193068441e-5
allele num: 11426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: -2.416e0

DP
type: SiteQuality
SIO_000300: 1.570068e6

QD
type: SiteQuality
SIO_000300: 4.28e0

FS
type: SiteQuality
SIO_000300: 5.171e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.446e0

GenotypeDepth
all individuals: 223
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6636
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 519
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47169
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1386
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510619656182966e-5
allele num: 66198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9974
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

DP
type: SiteQuality
SIO_000300: 1.573166e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.242e0

MQRankSum
type: SiteQuality
SIO_000300: -1.2e0

QD
type: SiteQuality
SIO_000300: 7.41e0

GenotypeDepth
all individuals: 21626
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6634
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 47115
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1119
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 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: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
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: 1
allele frequency: 8.733624454148471e-5
allele num: 11450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9980
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66224
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.090000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.574128e6

MQ
type: SiteQuality
SIO_000300: 5.867e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.951e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.964e0

QD
type: SiteQuality
SIO_000300: 7.74e0

GenotypeDepth
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 579
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47427
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6679
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1124
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1390
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66346
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.111722283339445e-5
allele num: 16362
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.656e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.579558e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.378e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.12e-1

QD
type: SiteQuality
SIO_000300: 8.24e0

GenotypeDepth
all individuals: 1289
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6684
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 514
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47568
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1392
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
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: 0
allele frequency: 0.0e0
allele num: 10090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.025729866530083e-5
allele num: 66382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.2e0

FS
type: SiteQuality
SIO_000300: 5.45e-1

DP
type: SiteQuality
SIO_000300: 1.580774e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

QD
type: SiteQuality
SIO_000300: 1.341e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

GenotypeDepth
all individuals: 1289
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 533
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66400
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.103515625e-5
allele num: 16384
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: 0
allele frequency: 0.0e0
allele num: 10098
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.908e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.99e-1

DP
type: SiteQuality
SIO_000300: 1.580964e6

VQSLOD
type: SiteQuality
SIO_000300: 1.42e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

QD
type: SiteQuality
SIO_000300: 1.285e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e0

GenotypeDepth
all individuals: 153
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 47535
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 553
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variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.024640780793445e-5
allele num: 66394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
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
allele num: 10094
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.113e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

FS
type: SiteQuality
SIO_000300: 8.412000000000001e0

DP
type: SiteQuality
SIO_000300: 1.581047e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.091e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

GenotypeDepth
all individuals: 102
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 6682
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1119
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variant carriers: 0

GenotypeQuality
all individuals: 600
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 47637
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variant carriers: 0

GenotypeQuality
all individuals: 508
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variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 1391
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
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variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50665943470138e-5
allele num: 66372
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: 0
allele frequency: 0.0e0
allele num: 10090
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
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: -3.9e-2

QD
type: SiteQuality
SIO_000300: 7.57e0

DP
type: SiteQuality
SIO_000300: 1.581197e6

VQSLOD
type: SiteQuality
SIO_000300: -1.907e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.95e0

FS
type: SiteQuality
SIO_000300: 7.61e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 262
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 12
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 504
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variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65678
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16200
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.4e-1

FS
type: SiteQuality
SIO_000300: 1.153e0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
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SIO_000300: -3.388e0

QD
type: SiteQuality
SIO_000300: 1.006e1

DP
type: SiteQuality
SIO_000300: 1.560949e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.8e-2

GenotypeDepth
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bin: 8.25e1
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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 111
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variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 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: 8630
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524901643843972e-5
allele num: 65578
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.096e0

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-2

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.17e0

FS
type: SiteQuality
SIO_000300: 1.936e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.558165e6

GenotypeDepth
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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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variant carriers: 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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GenotypeQuality
all individuals: 245
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GenotypeQuality
all individuals: 245
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11254
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9818
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.107243190423842e-5
allele num: 65496
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16158
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.004e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.56e-1

DP
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BaseQRankSum
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SIO_000300: 3.46e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 58
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variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
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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: 7.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 263
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GenotypeQuality
all individuals: 44776
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533883486210388e-5
allele num: 65194
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16088
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11182
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.237e1

DP
type: SiteQuality
SIO_000300: 1.548209e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-1

BaseQRankSum
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SIO_000300: -2.731e0

ReadPosRankSum
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SIO_000300: -1.062e0

FS
type: SiteQuality
SIO_000300: 7.323e0

VQSLOD
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SIO_000300: -1.937e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.54e-1

GenotypeDepth
all individuals: 58
bin: 8.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.099525772556799e-5
allele num: 64526
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15974
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.532493e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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SIO_000300: 1.305e1

FS
type: SiteQuality
SIO_000300: 8.4e-1

InbreedingCoeff
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SIO_000300: -7.0e-4

VQSLOD
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SIO_000300: 2.24e0

MQRankSum
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SIO_000300: 5.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.605e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 216
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10956
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.565190170605729e-5
allele num: 63890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.288e1

MQRankSum
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SIO_000300: 1.73e0

FS
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SIO_000300: 0.0e0

DP
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SIO_000300: 1.517246e6

VQSLOD
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SIO_000300: -4.479e-1

ReadPosRankSum
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SIO_000300: 2.12e0

BaseQRankSum
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SIO_000300: -4.373e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.734e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 116
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GenotypeQuality
all individuals: 1023
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6228
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.272102785905101e-4
allele num: 15722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10748
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62820
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.490163e6

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
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SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

BaseQRankSum
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SIO_000300: -2.437e0

VQSLOD
type: SiteQuality
SIO_000300: 7.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

QD
type: SiteQuality
SIO_000300: 1.303e1

GenotypeDepth
all individuals: 2920
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2498
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GenotypeQuality
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GenotypeQuality
all individuals: 451
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variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9126
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.320658342792281e-5
allele num: 56384
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.137138958380714e-4
allele num: 8794
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14978
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.471e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 2.53e0

ClippingRankSum
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SIO_000300: -6.56e-1

MQRankSum
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SIO_000300: 4.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

FS
type: SiteQuality
SIO_000300: 6.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

DP
type: SiteQuality
SIO_000300: 1.296476e6

VQSLOD
type: SiteQuality
SIO_000300: 3.06e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 2291
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8768
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.150262772156877e-5
allele num: 55942
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.71e-1

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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SIO_000300: 2.03e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.309e0

DP
type: SiteQuality
SIO_000300: 1.292618e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1981
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variant carriers: 1

GenotypeQuality
all individuals: 3032
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.97371018039711e-5
allele num: 50666
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7766
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6888
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5008
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.52e-1

InbreedingCoeff
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MQ
type: SiteQuality
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FS
type: SiteQuality
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DP
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VQSLOD
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QD
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BaseQRankSum
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SIO_000300: -1.178e0

MQRankSum
type: SiteQuality
SIO_000300: -9.6e-1

ReadPosRankSum
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SIO_000300: 2.18e0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 701
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GenotypeQuality
all individuals: 230
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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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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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East Asian
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South Asian
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allele frequency: 4.901274331326144e-4
allele num: 14282
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Latino
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MQ
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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DP
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QD
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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African
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South Asian
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allele frequency: 1.306681734708292e-2
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European (Finnish)
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East Asian
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VQSLOD
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MQ
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BaseQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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FS
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MQRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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South Asian
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VQSLOD
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MQ
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InbreedingCoeff
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DP
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QD
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FS
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

East Asian
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allele frequency: 0.0e0
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Other
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South Asian
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allele count: 2
allele frequency: 1.575299306868305e-4
allele num: 12696
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European (Finnish)
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allele count: 0
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African
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Latino
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
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BaseQRankSum
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QD
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FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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ClippingRankSum
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SIO_000300: -4.23e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele count: 0
allele frequency: 0.0e0
allele num: 5450
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 1.488095238095238e-4
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num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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South Asian
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Other
type: Population
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FS
type: SiteQuality
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MQ
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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VQSLOD
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QD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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allele frequency: 2.626395272488509e-3
allele num: 6092
num of homozygotes: 0

Latino
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allele frequency: 2.123142250530786e-4
allele num: 4710
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European (Finnish)
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allele count: 2
allele frequency: 5.807200929152149e-4
allele num: 3444
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European (Non-Finnish)
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allele frequency: 1.218296599844944e-3
allele num: 36116
num of homozygotes: 0

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

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

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

East Asian
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allele num: 8576
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Latino
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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allele num: 11372
num of homozygotes: 0

European (Finnish)
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East Asian
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African
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South Asian
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
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QD
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DP
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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FS
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ClippingRankSum
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InbreedingCoeff
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DP
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QD
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MQ
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VQSLOD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Other
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BaseQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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QD
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MQ
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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East Asian
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African
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European (Finnish)
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Other
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European (Non-Finnish)
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MQ
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BaseQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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DP
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VQSLOD
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SIO_000300: 9.320000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

FS
type: SiteQuality
SIO_000300: 6.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.74e-1

GenotypeQuality
all individuals: 562
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 274
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1793
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1328
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 333
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42988
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
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GenotypeQuality
all individuals: 302
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8146
bin: 6.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50793172085168e-5
allele num: 66316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

QD
type: SiteQuality
SIO_000300: 9.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 1.794748e6

MQRankSum
type: SiteQuality
SIO_000300: 1.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

GenotypeQuality
all individuals: 1788
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 160
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 850
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
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GenotypeQuality
all individuals: 198
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GenotypeQuality
all individuals: 1327
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 195
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
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GenotypeQuality
all individuals: 8219
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variant carriers: 0

GenotypeQuality
all individuals: 43673
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variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.74737578726382e-5
allele num: 11432
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.3207e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.2e-2

QD
type: SiteQuality
SIO_000300: 9.289999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: -9.4e-2

DP
type: SiteQuality
SIO_000300: 1.800804e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.816e1

VQSLOD
type: SiteQuality
SIO_000300: -1.795e0

GenotypeQuality
all individuals: 171
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 227
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 9.75e1
variant carriers: 107

GenotypeQuality
all individuals: 284
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variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 845
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 8232
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1781
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
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variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1636
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44326
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.257907542579075e-4
allele num: 16440
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.856145251396648e-4
allele num: 11456
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.217294900221729e-3
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.714396735962697e-5
allele num: 10294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 87
allele frequency: 1.309255079006772e-3
allele num: 66450
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e0

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

MQRankSum
type: SiteQuality
SIO_000300: 4.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

DP
type: SiteQuality
SIO_000300: 1.80946e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

FS
type: SiteQuality
SIO_000300: 1.216e0

QD
type: SiteQuality
SIO_000300: 1.39e1

MQ
type: SiteQuality
SIO_000300: 5.93e1

GenotypeDepth
all individuals: 61
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8310
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
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variant carriers: 0

GenotypeQuality
all individuals: 1300
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 302
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 486
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 1625
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variant carriers: 0

GenotypeQuality
all individuals: 1783
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variant carriers: 0

GenotypeQuality
all individuals: 363
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variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44940
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -5.904e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.03e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 9.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.228e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.814972e6

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

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

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
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variant carriers: 0

GenotypeQuality
all individuals: 45126
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variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
all individuals: 474
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variant carriers: 0

GenotypeQuality
all individuals: 8323
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 1623
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variant carriers: 0

GenotypeQuality
all individuals: 1298
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 103
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1767
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.006072265977274e-5
allele num: 66532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.253e1

DP
type: SiteQuality
SIO_000300: 1.817184e6

MQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.43e-1

FS
type: SiteQuality
SIO_000300: 1.695e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 157
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 45091
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1597
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variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 360
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variant carriers: 0

GenotypeQuality
all individuals: 8297
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1757
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 1
allele frequency: 8.706251088281386e-5
allele num: 11486
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.01e-1

QD
type: SiteQuality
SIO_000300: 1.605e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

DP
type: SiteQuality
SIO_000300: 1.817617e6

FS
type: SiteQuality
SIO_000300: 4.293e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.138e0

GenotypeQuality
all individuals: 570
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 300
bin: 8.75e1
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GenotypeQuality
all individuals: 45238
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8293
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1297
bin: 9.75e1
variant carriers: 2

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.706251088281386e-5
allele num: 11486
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502945773716484e-5
allele num: 66536
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.613e0

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

DP
type: SiteQuality
SIO_000300: 1.817882e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.129999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.09e1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1595
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variant carriers: 0

GenotypeQuality
all individuals: 827
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variant carriers: 0

GenotypeQuality
all individuals: 358
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 300
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variant carriers: 0

GenotypeQuality
all individuals: 83
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variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 570
bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502945773716484e-5
allele num: 66536
num of homozygotes: 0

ReadPosRankSum
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SIO_000300: -2.09e-1

MQRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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DP
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QD
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SIO_000300: 1.09e1

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.47e-1

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

East Asian
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allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.706251088281386e-5
allele num: 11486
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.503036132988637e-5
allele num: 66532
num of homozygotes: 0

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

FS
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ReadPosRankSum
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MQ
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BaseQRankSum
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QD
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MQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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SIO_000300: 9.3e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11484
num of homozygotes: 0

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

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

African
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allele count: 1
allele frequency: 9.68429207824908e-5
allele num: 10326
num of homozygotes: 0

Other
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.503397678753984e-5
allele num: 66516
num of homozygotes: 0

InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
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QD
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MQ
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MQRankSum
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DP
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FS
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ReadPosRankSum
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SIO_000300: -3.2e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 1
allele frequency: 1.503397678753984e-5
allele num: 66516
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

African
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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

East Asian
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -3.52e-1

MQ
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SIO_000300: 5.921e1

QD
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ClippingRankSum
type: SiteQuality
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VQSLOD
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DP
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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SIO_000300: -3.0e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16066
num of homozygotes: 0

East Asian
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allele frequency: 1.189060642092747e-4
allele num: 8410
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9438
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63978
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

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

QD
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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FS
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SIO_000300: 1.1826e1

MQ
type: SiteQuality
SIO_000300: 5.845e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.054738226349963e-5
allele num: 48668
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3920
num of homozygotes: 0

Latino
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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

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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QD
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InbreedingCoeff
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FS
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VQSLOD
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ReadPosRankSum
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MQRankSum
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DP
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BaseQRankSum
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GenotypeQuality
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variant carriers: 11

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10

Latino
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allele count: 577
allele frequency: 7.604111755403269e-2
allele num: 7588
num of homozygotes: 11

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7070
num of homozygotes: 0

European (Non-Finnish)
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allele count: 37
allele frequency: 7.602531437494863e-4
allele num: 48668
num of homozygotes: 0

East Asian
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allele frequency: 1.521606816798539e-4
allele num: 6572
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European (Finnish)
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allele frequency: 5.102040816326531e-4
allele num: 3920
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South Asian
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allele frequency: 4.469887076537014e-3
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Other
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FS
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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QD
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 7.841907151819322e-5
allele num: 12752
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7070
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48668
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3920
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.144946e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.17e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.12e0

QD
type: SiteQuality
SIO_000300: 1.887e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

GenotypeQuality
all individuals: 2219
bin: 3.75e1
variant carriers: 1007

GenotypeQuality
all individuals: 1280
bin: 6.75e1
variant carriers: 558

GenotypeQuality
all individuals: 928
bin: 7.75e1
variant carriers: 661

GenotypeQuality
all individuals: 1682
bin: 4.25e1
variant carriers: 1088

GenotypeQuality
all individuals: 2834
bin: 3.25e1
variant carriers: 915

GenotypeQuality
all individuals: 4861
bin: 2.25e1
variant carriers: 828

GenotypeQuality
all individuals: 2354
bin: 6.25e1
variant carriers: 556

GenotypeQuality
all individuals: 1382
bin: 4.75e1
variant carriers: 886

GenotypeQuality
all individuals: 1725
bin: 1.25e1
variant carriers: 647

GenotypeQuality
all individuals: 1530
bin: 1.75e1
variant carriers: 797

GenotypeQuality
all individuals: 22324
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variant carriers: 21634

GenotypeQuality
all individuals: 596
bin: 9.25e1
variant carriers: 519

GenotypeQuality
all individuals: 825
bin: 8.75e1
variant carriers: 738

GenotypeQuality
all individuals: 940
bin: 8.25e1
variant carriers: 753

GenotypeQuality
all individuals: 902
bin: 7.25e1
variant carriers: 610

GenotypeQuality
all individuals: 3320
bin: 2.75e1
variant carriers: 1049

GenotypeQuality
all individuals: 6591
bin: 2.5e0
variant carriers: 450

GenotypeQuality
all individuals: 2168
bin: 7.5e0
variant carriers: 427

GenotypeQuality
all individuals: 1239
bin: 5.25e1
variant carriers: 994

GenotypeQuality
all individuals: 843
bin: 5.75e1
variant carriers: 701

European (Finnish)
type: Population
allele count: 1692
allele frequency: 4.316326530612245e-1
allele num: 3920
num of homozygotes: 351

European (Non-Finnish)
type: Population
allele count: 18441
allele frequency: 3.789142763211967e-1
allele num: 48668
num of homozygotes: 2649

South Asian
type: Population
allele count: 4306
allele frequency: 3.3767252195734e-1
allele num: 12752
num of homozygotes: 486

African
type: Population
allele count: 4096
allele frequency: 5.793493635077793e-1
allele num: 7070
num of homozygotes: 1103

Latino
type: Population
allele count: 3217
allele frequency: 4.239588824459673e-1
allele num: 7588
num of homozygotes: 542

East Asian
type: Population
allele count: 2765
allele frequency: 4.207242848447961e-1
allele num: 6572
num of homozygotes: 490

Other
type: Population
allele count: 244
allele frequency: 3.742331288343558e-1
allele num: 652
num of homozygotes: 38

VQSLOD
type: SiteQuality
SIO_000300: 5.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.887e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.17e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

DP
type: SiteQuality
SIO_000300: 1.144946e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2354
bin: 6.25e1
variant carriers: 14

GenotypeQuality
all individuals: 1530
bin: 1.75e1
variant carriers: 11

GenotypeQuality
all individuals: 843
bin: 5.75e1
variant carriers: 19

GenotypeQuality
all individuals: 2834
bin: 3.25e1
variant carriers: 13

GenotypeQuality
all individuals: 1239
bin: 5.25e1
variant carriers: 28

GenotypeQuality
all individuals: 928
bin: 7.75e1
variant carriers: 21

GenotypeQuality
all individuals: 2219
bin: 3.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1725
bin: 1.25e1
variant carriers: 22

GenotypeQuality
all individuals: 4861
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variant carriers: 13

GenotypeQuality
all individuals: 940
bin: 8.25e1
variant carriers: 12

GenotypeQuality
all individuals: 3320
bin: 2.75e1
variant carriers: 9

GenotypeQuality
all individuals: 825
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variant carriers: 9

GenotypeQuality
all individuals: 2168
bin: 7.5e0
variant carriers: 8

GenotypeQuality
all individuals: 6591
bin: 2.5e0
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GenotypeQuality
all individuals: 1382
bin: 4.75e1
variant carriers: 23

GenotypeQuality
all individuals: 1280
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variant carriers: 18

GenotypeQuality
all individuals: 1682
bin: 4.25e1
variant carriers: 12

GenotypeQuality
all individuals: 22324
bin: 9.75e1
variant carriers: 35

GenotypeQuality
all individuals: 902
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variant carriers: 30

GenotypeQuality
all individuals: 596
bin: 9.25e1
variant carriers: 7

East Asian
type: Population
allele count: 25
allele frequency: 3.804017041996348e-3
allele num: 6572
num of homozygotes: 0

Latino
type: Population
allele count: 19
allele frequency: 2.503953610964681e-3
allele num: 7588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 128
allele frequency: 2.630064929727953e-3
allele num: 48668
num of homozygotes: 0

South Asian
type: Population
allele count: 48
allele frequency: 3.764115432873275e-3
allele num: 12752
num of homozygotes: 0

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

African
type: Population
allele count: 29
allele frequency: 4.101838755304102e-3
allele num: 7070
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 19
allele frequency: 4.846938775510204e-3
allele num: 3920
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.17e-2

QD
type: SiteQuality
SIO_000300: 1.887e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 1.144946e6

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 694
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30943
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1135
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1002
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variant carriers: 0

GenotypeQuality
all individuals: 52
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variant carriers: 0

GenotypeQuality
all individuals: 2027
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variant carriers: 0

GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 378
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GenotypeQuality
all individuals: 1791
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5702
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1082
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.060728744939271e-4
allele num: 1976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16764
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2236
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.01e-1

QD
type: SiteQuality
SIO_000300: 1.568e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

MQ
type: SiteQuality
SIO_000300: 6.091e1

VQSLOD
type: SiteQuality
SIO_000300: 1.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

FS
type: SiteQuality
SIO_000300: 2.522e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.361386e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.812e-1

GenotypeQuality
all individuals: 1488
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12277
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variant carriers: 0

GenotypeQuality
all individuals: 2460
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GenotypeQuality
all individuals: 2280
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variant carriers: 0

GenotypeQuality
all individuals: 6793
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variant carriers: 0

GenotypeQuality
all individuals: 274
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variant carriers: 0

GenotypeQuality
all individuals: 994
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variant carriers: 0

GenotypeQuality
all individuals: 1990
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variant carriers: 0

GenotypeQuality
all individuals: 2558
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variant carriers: 0

GenotypeQuality
all individuals: 8031
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GenotypeQuality
all individuals: 586
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variant carriers: 0

GenotypeQuality
all individuals: 2525
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variant carriers: 0

GenotypeQuality
all individuals: 1048
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GenotypeQuality
all individuals: 1388
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variant carriers: 0

GenotypeQuality
all individuals: 7019
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variant carriers: 0

GenotypeQuality
all individuals: 513
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variant carriers: 0

GenotypeQuality
all individuals: 5472
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variant carriers: 0

GenotypeQuality
all individuals: 264
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variant carriers: 0

GenotypeQuality
all individuals: 950
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variant carriers: 0

GenotypeQuality
all individuals: 1308
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56180
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.318565400843882e-4
allele num: 7584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7944
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9462
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

QD
type: SiteQuality
SIO_000300: 3.2e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.92e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e0

MQRankSum
type: SiteQuality
SIO_000300: -2.74e-1

DP
type: SiteQuality
SIO_000300: 1.180474e6

GenotypeQuality
all individuals: 1315
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 993
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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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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 275
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GenotypeQuality
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GenotypeQuality
all individuals: 12039
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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: 978
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GenotypeQuality
all individuals: 2199
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2653
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7097
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2480
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 266
bin: 8.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7910
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.935911641705687e-5
allele num: 55954
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.01e0

MQRankSum
type: SiteQuality
SIO_000300: -1.08e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.976e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

QD
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.699999999999999e-3

FS
type: SiteQuality
SIO_000300: 5.5591e1

DP
type: SiteQuality
SIO_000300: 1.179209e6

GenotypeQuality
all individuals: 1328
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 307
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variant carriers: 1

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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GenotypeQuality
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GenotypeQuality
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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: 432
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GenotypeQuality
all individuals: 12184
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1563
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 676
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.715052638917939e-5
allele num: 57372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5286
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-3

DP
type: SiteQuality
SIO_000300: 1.222734e6

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.625e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.4098e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 30

GenotypeQuality
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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: 23

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 18

GenotypeQuality
all individuals: 1087
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variant carriers: 190

GenotypeQuality
all individuals: 562
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GenotypeQuality
all individuals: 825
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variant carriers: 13

GenotypeQuality
all individuals: 3169
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variant carriers: 20

GenotypeQuality
all individuals: 383
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variant carriers: 8

GenotypeQuality
all individuals: 11510
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GenotypeQuality
all individuals: 2695
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variant carriers: 35

GenotypeQuality
all individuals: 2381
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variant carriers: 15

GenotypeQuality
all individuals: 1646
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variant carriers: 12

GenotypeQuality
all individuals: 5399
bin: 2.75e1
variant carriers: 29

GenotypeQuality
all individuals: 169
bin: 9.25e1
variant carriers: 7

European (Finnish)
type: Population
allele count: 29
allele frequency: 9.904371584699454e-3
allele num: 2928
num of homozygotes: 1

South Asian
type: Population
allele count: 8
allele frequency: 5.971931919976113e-4
allele num: 13396
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 5.597014925373134e-3
allele num: 536
num of homozygotes: 0

African
type: Population
allele count: 25
allele frequency: 5.02411575562701e-3
allele num: 4976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 279
allele frequency: 6.761997091614154e-3
allele num: 41260
num of homozygotes: 0

Latino
type: Population
allele count: 26
allele frequency: 4.464285714285714e-3
allele num: 5824
num of homozygotes: 0

East Asian
type: Population
allele count: 25
allele frequency: 4.787437763309077e-3
allele num: 5222
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.283e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.05e-1

FS
type: SiteQuality
SIO_000300: 8.9102e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.646e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.875e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

QD
type: SiteQuality
SIO_000300: 2.23e0

DP
type: SiteQuality
SIO_000300: 1.197984e6

GenotypeQuality
all individuals: 5868
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5399
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2609
bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11510
bin: 2.5e0
variant carriers: 101

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 825
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1458
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1646
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3169
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3313
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8420
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4976
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.423654871546292e-5
allele num: 41260
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.914975105323631e-4
allele num: 5222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 3.415300546448087e-4
allele num: 2928
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.05e-1

QD
type: SiteQuality
SIO_000300: 2.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.875e0

VQSLOD
type: SiteQuality
SIO_000300: -5.646e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.283e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.56e-1

FS
type: SiteQuality
SIO_000300: 8.9102e1

DP
type: SiteQuality
SIO_000300: 1.197984e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

GenotypeQuality
all individuals: 11510
bin: 2.5e0
variant carriers: 257

GenotypeQuality
all individuals: 4212
bin: 3.75e1
variant carriers: 45

GenotypeQuality
all individuals: 3313
bin: 1.75e1
variant carriers: 105

GenotypeQuality
all individuals: 1087
bin: 9.75e1
variant carriers: 24

GenotypeQuality
all individuals: 1458
bin: 6.75e1
variant carriers: 8

GenotypeQuality
all individuals: 5868
bin: 3.25e1
variant carriers: 51

GenotypeQuality
all individuals: 8420
bin: 2.25e1
variant carriers: 85

GenotypeQuality
all individuals: 2381
bin: 4.75e1
variant carriers: 23

GenotypeQuality
all individuals: 383
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2229
bin: 4.25e1
variant carriers: 39

GenotypeQuality
all individuals: 3169
bin: 6.25e1
variant carriers: 7

GenotypeQuality
all individuals: 562
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2609
bin: 7.5e0
variant carriers: 178

GenotypeQuality
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bin: 1.25e1
variant carriers: 131

GenotypeQuality
all individuals: 5399
bin: 2.75e1
variant carriers: 87

GenotypeQuality
all individuals: 1646
bin: 5.25e1
variant carriers: 17

GenotypeQuality
all individuals: 201
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 645
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 169
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 825
bin: 5.75e1
variant carriers: 16

African
type: Population
allele count: 62
allele frequency: 1.245980707395498e-2
allele num: 4976
num of homozygotes: 0

Latino
type: Population
allele count: 23
allele frequency: 3.949175824175824e-3
allele num: 5824
num of homozygotes: 0

Other
type: Population
allele count: 7
allele frequency: 1.305970149253731e-2
allele num: 536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 24
allele frequency: 8.19672131147541e-3
allele num: 2928
num of homozygotes: 1

East Asian
type: Population
allele count: 36
allele frequency: 6.89391037916507e-3
allele num: 5222
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 7.464914899970141e-4
allele num: 13396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 216
allele frequency: 5.23509452253999e-3
allele num: 41260
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.875e0

FS
type: SiteQuality
SIO_000300: 8.9102e1

MQ
type: SiteQuality
SIO_000300: 5.934e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.283e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.646e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

DP
type: SiteQuality
SIO_000300: 1.197984e6

GenotypeQuality
all individuals: 1258
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1598
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5805
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variant carriers: 0

GenotypeQuality
all individuals: 3190
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variant carriers: 0

GenotypeQuality
all individuals: 9894
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variant carriers: 0

GenotypeQuality
all individuals: 1389
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variant carriers: 0

GenotypeQuality
all individuals: 6129
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variant carriers: 0

GenotypeQuality
all individuals: 2599
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3050
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variant carriers: 0

GenotypeQuality
all individuals: 1413
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GenotypeQuality
all individuals: 5694
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variant carriers: 0

GenotypeQuality
all individuals: 1363
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variant carriers: 0

GenotypeQuality
all individuals: 483
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GenotypeQuality
all individuals: 2757
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variant carriers: 0

GenotypeQuality
all individuals: 2206
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GenotypeQuality
all individuals: 7439
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variant carriers: 0

GenotypeQuality
all individuals: 402
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variant carriers: 0

GenotypeQuality
all individuals: 2177
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57692
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8856
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.64451827242525e-5
allele num: 15050
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.684e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.589e0

DP
type: SiteQuality
SIO_000300: 1.345783e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.0e-1

FS
type: SiteQuality
SIO_000300: 6.502e0

VQSLOD
type: SiteQuality
SIO_000300: -2.251e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.12e-2

QD
type: SiteQuality
SIO_000300: 6.48e0

GenotypeQuality
all individuals: 184
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

GenotypeQuality
all individuals: 523
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variant carriers: 0

GenotypeQuality
all individuals: 3817
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 4157
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variant carriers: 1

GenotypeQuality
all individuals: 387
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variant carriers: 0

GenotypeQuality
all individuals: 3179
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variant carriers: 0

GenotypeQuality
all individuals: 125
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variant carriers: 0

GenotypeQuality
all individuals: 123
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variant carriers: 0

GenotypeQuality
all individuals: 1417
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variant carriers: 0

GenotypeQuality
all individuals: 9715
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variant carriers: 0

GenotypeQuality
all individuals: 31525
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variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2491
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variant carriers: 0

GenotypeQuality
all individuals: 1030
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variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.573663173134422e-5
allele num: 63546
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9332
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16250
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.83e-1

DP
type: SiteQuality
SIO_000300: 1.784471e6

QD
type: SiteQuality
SIO_000300: 1.092e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.389999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

GenotypeQuality
all individuals: 4157
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 508
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variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 385
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variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 119
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variant carriers: 0

GenotypeQuality
all individuals: 3175
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variant carriers: 0

GenotypeQuality
all individuals: 31600
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variant carriers: 0

GenotypeQuality
all individuals: 1416
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variant carriers: 0

GenotypeQuality
all individuals: 9705
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variant carriers: 0

GenotypeQuality
all individuals: 126
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variant carriers: 0

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 2483
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variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

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

GenotypeQuality
all individuals: 3810
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16252
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.869306556706224e-5
allele num: 63538
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9334
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.52e-1

DP
type: SiteQuality
SIO_000300: 1.785032e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.796e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.79e-1

FS
type: SiteQuality
SIO_000300: 8.587999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

QD
type: SiteQuality
SIO_000300: 1.142e1

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.75e-1

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3808
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 396
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 9707
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 4150
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 31890
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.573514602215509e-5
allele num: 63552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9330
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16254
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.85e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 1.0847e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-2

QD
type: SiteQuality
SIO_000300: 1.177e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.781e0

MQRankSum
type: SiteQuality
SIO_000300: -5.03e-1

DP
type: SiteQuality
SIO_000300: 1.785987e6

VQSLOD
type: SiteQuality
SIO_000300: -1.272e0

GenotypeQuality
all individuals: 9717
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 29
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 77
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GenotypeQuality
all individuals: 31992
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GenotypeQuality
all individuals: 4150
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variant carriers: 1

GenotypeQuality
all individuals: 1416
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variant carriers: 0

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

GenotypeQuality
all individuals: 1028
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.072041166380789e-4
allele num: 9328
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.79e-1

DP
type: SiteQuality
SIO_000300: 1.786744e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.88e-1

FS
type: SiteQuality
SIO_000300: 4.694e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

QD
type: SiteQuality
SIO_000300: 1.059e1

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 2484
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variant carriers: 0

GenotypeQuality
all individuals: 4149
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 32116
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9723
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3790
bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9330
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.471e0

QD
type: SiteQuality
SIO_000300: 1.319e1

DP
type: SiteQuality
SIO_000300: 1.788154e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

MQRankSum
type: SiteQuality
SIO_000300: 7.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

GenotypeQuality
all individuals: 1413
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3789
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 80
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3177
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32263
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4142
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9717
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2475
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.573019568363431e-5
allele num: 63572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

European (Finnish)
type: Population
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
allele num: 8514
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: 0
allele frequency: 0.0e0
allele num: 9326
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.715e0

FS
type: SiteQuality
SIO_000300: 2.315e0

DP
type: SiteQuality
SIO_000300: 1.788974e6

QD
type: SiteQuality
SIO_000300: 2.802e1

MQRankSum
type: SiteQuality
SIO_000300: -4.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.837e0

GenotypeDepth
all individuals: 329
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 313
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3789
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 489
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3174
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9714
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2474
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32288
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4142
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1413
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.573118550213944e-5
allele num: 63568
num of homozygotes: 0

European (Finnish)
type: Population
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
allele num: 8516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9322
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: 11454
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.218e1

VQSLOD
type: SiteQuality
SIO_000300: -8.612e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

MQRankSum
type: SiteQuality
SIO_000300: -1.767e0

DP
type: SiteQuality
SIO_000300: 1.789201e6

GenotypeDepth
all individuals: 4819
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3175
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4141
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1413
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9715
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3790
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2476
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32287
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.573069057731634e-5
allele num: 63570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16264
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

VQSLOD
type: SiteQuality
SIO_000300: 6.58e-1

QD
type: SiteQuality
SIO_000300: 1.301e1

MQ
type: SiteQuality
SIO_000300: 5.942e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

DP
type: SiteQuality
SIO_000300: 1.789192e6

FS
type: SiteQuality
SIO_000300: 6.295e0

MQRankSum
type: SiteQuality
SIO_000300: 4.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-2