7-73152030-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152030
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152030
    reference: chr 7
allele count: 6
allele frequency: 5.026135906714917e-5
allele num: 119376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*227C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.303C>T
  hgvsp: ENST00000437775.2:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.219C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.324C>T
  hgvsp: ENST00000222800.3:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.324C>T
  hgvsp: ENST00000458339.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.*13C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.266C>T
  hgvsp: ENST00000412965.1:c.266C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.716C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.359C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.172C>T
  hgvsp: ENST00000437891.1:c.172C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.324C>T
  hgvsp: ENST00000395147.4:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.303C>T
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser108Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

7-73152033-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152033
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152033
    reference: chr 7
allele count: 7
allele frequency: 5.878993516310008e-5
allele num: 119068
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.263C>G
  hgvsp: ENSP00000387908.1:p.Asp88Glu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.300C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.321C>G
  hgvsp: ENSP00000222800.3:p.Asp107Glu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.321C>G
  hgvsp: ENSP00000397666.1:p.Asp107Glu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.713C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.169C>G
  hgvsp: ENSP00000410536.1:p.Asp57Glu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.356C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.300C>G
  hgvsp: ENSP00000416970.2:p.Asp100Glu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.*10C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.216C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*224C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.321C>G
  hgvsp: ENSP00000378579.4:p.Asp107Glu
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28579
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp107Glu
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

7-73152038-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152038
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152038
    reference: chr 7
allele count: 1
allele frequency: 8.428434165500733e-6
allele num: 118646
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*219G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.316G>A
  hgvsp: ENSP00000378579.4:p.Gly106Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.351G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.258G>A
  hgvsp: ENSP00000387908.1:p.Gly87Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.316G>A
  hgvsp: ENSP00000222800.3:p.Gly106Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.211G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.164G>A
  hgvsp: ENSP00000410536.1:p.Gly56Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.295G>A
  hgvsp: ENSP00000416970.2:p.Gly99Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.295G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.316G>A
  hgvsp: ENSP00000397666.1:p.Gly106Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.708G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.*5G>A
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly106Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

7-73152041-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152041
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152041
    reference: chr 7
allele count: 5
allele frequency: 4.221760643058581e-5
allele num: 118434
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.348C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.313C>G
  hgvsp: ENSP00000397666.1:p.His105Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.313C>G
  hgvsp: ENSP00000222800.3:p.His105Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.*2C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.313C>G
  hgvsp: ENSP00000378579.4:p.His105Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.292C>G
  hgvsp: ENSP00000416970.2:p.His98Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.292C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.208C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.161C>G
  hgvsp: ENSP00000410536.1:p.His55Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.255C>G
  hgvsp: ENSP00000387908.1:p.His86Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*216C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.705C>G
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His105Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

7-73152047-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152047
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152047
    reference: chr 7
allele count: 2
allele frequency: 1.69537501695375e-5
allele num: 117968
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.699C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.307C>T
  hgvsp: ENSP00000378579.4:p.Arg103Cys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.155C>T
  hgvsp: ENSP00000410536.1:p.Arg53Cys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.307C>T
  hgvsp: ENSP00000397666.1:p.Arg103Cys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.249C>T
  hgvsp: ENSP00000387908.1:p.Arg84Cys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.286C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*210C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.748C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.307C>T
  hgvsp: ENSP00000222800.3:p.Arg103Cys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.302C>T
  hgvsp: ENSP00000392945.2:p.Ser101Leu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.286C>T
  hgvsp: ENSP00000416970.2:p.Arg96Cys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.342C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.202C>T
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4724
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg103Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

7-73152051-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152051
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152051
    reference: chr 7
allele count: 1
allele frequency: 8.521516829995738e-6
allele num: 117350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.151T>C
  hgvsp: ENST00000437891.1:c.151T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.298T>C
  hgvsp: ENSP00000392945.2:p.Cys100Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.245T>C
  hgvsp: ENST00000412965.1:c.245T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*206T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.303T>C
  hgvsp: ENST00000395147.4:c.303T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.744T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.282T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.695T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.338T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.303T>C
  hgvsp: ENST00000458339.1:c.303T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.303T>C
  hgvsp: ENST00000222800.3:c.303T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.198T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.282T>C
  hgvsp: ENST00000437775.2:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys100Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

7-73152057-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152057
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152057
    reference: chr 7
allele count: 1
allele frequency: 8.560617734175697e-6
allele num: 116814
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.297G>A
  hgvsp: ENST00000458339.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.239G>A
  hgvsp: ENST00000412965.1:c.239G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.689G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.297G>A
  hgvsp: ENST00000222800.3:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.276G>A
  hgvsp: ENST00000437775.2:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*200G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.297G>A
  hgvsp: ENST00000395147.4:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.292G>A
  hgvsp: ENSP00000392945.2:p.Gly98Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.145G>A
  hgvsp: ENST00000437891.1:c.145G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.332G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.192G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.276G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.738G>A
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly98Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

7-73152058-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152058
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152058
    reference: chr 7
allele count: 1
allele frequency: 8.570742911995611e-6
allele num: 116676
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.296C>T
  hgvsp: ENSP00000222800.3:p.Thr99Met
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.238C>T
  hgvsp: ENSP00000387908.1:p.Thr80Met
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.291C>T
  hgvsp: ENST00000357419.4:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.296C>T
  hgvsp: ENSP00000378579.4:p.Thr99Met
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.144C>T
  hgvsp: ENSP00000410536.1:p.Thr49Met
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.296C>T
  hgvsp: ENSP00000397666.1:p.Thr99Met
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.688C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*199C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.331C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.191C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.275C>T
  hgvsp: ENSP00000416970.2:p.Thr92Met
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.737C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.275C>T
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr99Met
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

7-73152058-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152058
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152058
    reference: chr 7
allele count: 1
allele frequency: 8.570742911995611e-6
allele num: 116676
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.296C>G
  hgvsp: ENSP00000397666.1:p.Thr99Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.291C>G
  hgvsp: ENSP00000392945.2:p.Asp97Glu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.144C>G
  hgvsp: ENSP00000410536.1:p.Thr49Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.688C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.275C>G
  hgvsp: ENSP00000416970.2:p.Thr92Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.296C>G
  hgvsp: ENSP00000378579.4:p.Thr99Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.275C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.737C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.296C>G
  hgvsp: ENSP00000222800.3:p.Thr99Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.191C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*199C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.238C>G
  hgvsp: ENSP00000387908.1:p.Thr80Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.331C>G
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr99Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

7-73152059-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152059
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152059
    reference: chr 7
allele count: 1
allele frequency: 8.568833439015613e-6
allele num: 116702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.290A>T
  hgvsp: ENSP00000392945.2:p.Asp97Val
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.736A>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.274A>T
  hgvsp: ENSP00000416970.2:p.Thr92Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*198A>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.190A>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.295A>T
  hgvsp: ENSP00000378579.4:p.Thr99Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.274A>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.330A>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.295A>T
  hgvsp: ENSP00000397666.1:p.Thr99Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.295A>T
  hgvsp: ENSP00000222800.3:p.Thr99Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.237A>T
  hgvsp: ENSP00000387908.1:p.Thr80Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.143A>T
  hgvsp: ENSP00000410536.1:p.Thr49Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.687A>T
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr99Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

7-73152071-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152071
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152071
    reference: chr 7
allele count: 1
allele frequency: 8.695047301057318e-6
allele num: 115008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.289-6C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.324-6C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.137-6C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.184-6C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*192-6C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.231-6C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.289-6C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.675C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.284-6C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.268-6C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.724C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.289-6C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.268-6C>T
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.289-6C>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

7-73152073-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152073
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152073
    reference: chr 7
allele count: 8
allele frequency: 6.958942240779402e-5
allele num: 114960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.673C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.722C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.268-8C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.289-8C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.184-8C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.289-8C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.284-8C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.268-8C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.289-8C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*192-8C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.324-8C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.231-8C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.137-8C>T
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20857
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.289-8C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

7-73152075-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152075
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152075
    reference: chr 7
allele count: 1
allele frequency: 8.781790080089925e-6
allele num: 113872
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.720C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.289-10C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.268-10C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.137-10C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.268-10C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.284-10C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.671C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.289-10C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.231-10C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.184-10C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.289-10C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*192-10C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.324-10C>G
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19890
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

7-73152091-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152091
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152091
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 111130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.704C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.289-26C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.284-26C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.231-26C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.289-26C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.184-26C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.289-26C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.268-26C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.655C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.137-26C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*192-26C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.324-26C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.268-26C>T
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

7-73152093-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152093
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152093
    reference: chr 7
allele count: 15
allele frequency: 1.355821899235317e-4
allele num: 110634
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.137-28C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.702C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.289-28C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.289-28C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.184-28C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.268-28C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.268-28C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.653C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*192-28C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.231-28C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.289-28C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.284-28C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.324-28C>T
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15345
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17995
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10645
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

7-73152097-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152097
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152097
    reference: chr 7
allele count: 3
allele frequency: 2.722174836215814e-5
allele num: 110206
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.289-32T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.698T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.324-32T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.649T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.231-32T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.137-32T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.289-32T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.268-32T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.268-32T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.284-32T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.184-32T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.289-32T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*192-32T>C
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7904
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16467
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-73152108-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152108
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152108
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 108052
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*192-43G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.184-43G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.268-43G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.137-43G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.268-43G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.687G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.289-43G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.289-43G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.289-43G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.638G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.324-43G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.231-43G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.284-43G>C
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 13109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5157
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

7-73152110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152110
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152110
    reference: chr 7
allele count: 4
allele frequency: 3.715952584445023e-5
allele num: 107644
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.289-45C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.324-45C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.268-45C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.231-45C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.289-45C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.636C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*192-45C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.685C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.289-45C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.284-45C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.137-45C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.268-45C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.184-45C>T
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14831
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

7-73152114-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152114
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152114
    reference: chr 7
allele count: 1
allele frequency: 9.382623381497466e-6
allele num: 106580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.289-49C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.289-49C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.681C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.231-49C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*192-49C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.289-49C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.184-49C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.632C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.324-49C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.284-49C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.137-49C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.268-49C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.268-49C>A
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14699
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

7-73152115-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152115
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152115
    reference: chr 7
allele count: 1
allele frequency: 9.379983116030392e-6
allele num: 106610
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.268-50A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.289-50A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.680A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.284-50A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.289-50A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.231-50A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.631A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.184-50A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*192-50A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.324-50A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.268-50A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.289-50A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.137-50A>G
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14660
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

7-73152350-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152350
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152350
    reference: chr 7
allele count: 31
allele frequency: 1.578572156024035e-3
allele num: 19638
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.179A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.137-285A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.231-285A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.268-285A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.289-285A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.445A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.289-285A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.268-285A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.284-285A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*47A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.289-285A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.184-285A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.396A>G
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

7-73152363-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152363
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152363
    reference: chr 7
allele count: 1
allele frequency: 5.104645227156713e-5
allele num: 19590
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.284-298C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*34C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+295C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+295C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.166C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+295C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.268-298C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+295C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+295C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.432C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+295C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.383C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+295C>A
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-73152364-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152364
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152364
    reference: chr 7
allele count: 1
allele frequency: 5.103082261686059e-5
allele num: 19596
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+294T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.165T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+294T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+294T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+299T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.431T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.382T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+294T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+294T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+299T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*33T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+294T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+294T>A
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: A
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

7-73152369-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152369
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152369
    reference: chr 7
allele count: 1
allele frequency: 5.150922015040692e-5
allele num: 19414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+289C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+289C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+289C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+289C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+289C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.377C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+294C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.160C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*28C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+294C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+289C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.426C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+289C>T
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3685
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

7-73152374-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152374
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152374
    reference: chr 7
allele count: 38
allele frequency: 1.941747572815534e-3
allele num: 19570
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+289G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.155G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+284G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+284G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+284G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*23G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+284G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.421G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.372G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+284G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+289G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+284G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+284G>A
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

7-73152377-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152377
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152377
    reference: chr 7
allele count: 2
allele frequency: 1.021972406745018e-4
allele num: 19570
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+281T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+281T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.152T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.418T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+286T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+281T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.*20T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.369T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+286T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+281T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+281T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+281T>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+281T>A
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ

7-73152399-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152399
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152399
    reference: chr 7
allele count: 1
allele frequency: 5.125576627370579e-5
allele num: 19510
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.396T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+259T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+259T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+259T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+259T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+259T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.130T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.262T>C
  hgvsp: ENSP00000430937.1:p.Ter88ArgextTer66
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+264T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+264T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.347T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+259T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+259T>C
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter88ArgextTer66
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

7-73152435-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152435
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152435
    reference: chr 7
allele count: 4
allele frequency: 2.057189878625797e-4
allele num: 19444
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+228C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+228C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+223C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+223C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+223C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.259-33C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+223C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.360C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+223C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.94C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+223C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+223C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.344-33C>A
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD

7-73152442-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152442
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152442
    reference: chr 7
allele count: 3
allele frequency: 1.543527474789051e-4
allele num: 19436
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.87G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+216G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+216G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+221G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.353G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+216G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+221G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+216G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+216G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+216G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+216G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.259-40G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.344-40G>A
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6510
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

7-73152615-T-TCCCGCCCAGCCCCAAAGGAGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152615
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152636
    reference: chr 7
allele count: 1
allele frequency: 1.172223003704225e-5
allele num: 85308
alternate allele: TCCCGCCCAGCCCCAAAGGAGC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9867
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21416
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

7-73152615-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152615
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152614
    reference: chr 7
allele count: 6
allele frequency: 7.033338022225348e-5
allele num: 85308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+42delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+42delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+42delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+42delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+42delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.258+42delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+47delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.343+42delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+47delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.56+42delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+42delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.322+42delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+42delG
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21416
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9867
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8595
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: TC
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-73152619-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152619
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152619
    reference: chr 7
allele count: 3
allele frequency: 3.54769281710461e-5
allele num: 84562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.258+39C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.343+39C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+39C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+39C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+39C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+39C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.322+39C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+44C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+39C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+39C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+44C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.56+39C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+39C>T
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8412
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20659
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

7-73152620-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152620
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152620
    reference: chr 7
allele count: 1
allele frequency: 1.146079262841818e-5
allele num: 87254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+43G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+43G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+38G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+38G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.322+38G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+38G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+38G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+38G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+38G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+38G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.258+38G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.343+38G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.56+38G>A
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14513
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

7-73152622-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152622
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152622
    reference: chr 7
allele count: 5
allele frequency: 5.682851427532279e-5
allele num: 87984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+36G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+36G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+41G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+36G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.322+36G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+36G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+41G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+36G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.56+36G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.258+36G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+36G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.343+36G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+36G>A
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18943
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14973
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14513
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6079
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

7-73152624-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152624
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152625
    reference: chr 7
allele count: 1
allele frequency: 1.131887535654457e-5
allele num: 88348
alternate allele: GC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+33dupG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+38dupG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.322+33dupG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+38dupG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.258+33dupG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+33dupG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.343+33dupG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+33dupG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+33dupG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.56+33dupG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+33dupG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+33dupG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+33dupG
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

7-73152625-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152625
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152625
    reference: chr 7
allele count: 9
allele frequency: 1.013011570843276e-4
allele num: 88844
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+33G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+33G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.258+33G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+38G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+33G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.56+33G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+33G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.322+33G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+33G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+33G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+38G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.343+33G>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+33G>C
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17600
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14349
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17454
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

7-73152625-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152625
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152625
    reference: chr 7
allele count: 21
allele frequency: 2.363693665300977e-4
allele num: 88844
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+33G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+33G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+33G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+38G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+38G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+33G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+33G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.322+33G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.343+33G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+33G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+33G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.258+33G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.56+33G>A
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17454
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17600
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14349
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/7-73152628-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152628
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152629
    reference: chr 7
allele count: 2
allele frequency: 2.222567955015225e-5
allele num: 89986
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+29dupT
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+29dupT
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.322+29dupT
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+29dupT
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.56+29dupT
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.258+29dupT
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+29dupT
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+29dupT
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+34dupT
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.343+29dupT
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+29dupT
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+34dupT
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+29dupT
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

7-73152635-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152635
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152634
    reference: chr 7
allele count: 1
allele frequency: 1.075870379136722e-5
allele num: 92948
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+22delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+22delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+27delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+22delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+27delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+22delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.258+22delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.56+22delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.343+22delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+22delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+22delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.322+22delG
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+22delG
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25497
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: GC
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum

7-73152641-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152641
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152641
    reference: chr 7
allele count: 1
allele frequency: 1.037043182478118e-5
allele num: 96428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+22G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+17G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+17G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.343+17G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.322+17G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+17G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+17G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.258+17G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+17G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.56+17G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+17G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+17G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+22G>A
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9077
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

7-73152646-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152646
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152646
    reference: chr 7
allele count: 2
allele frequency: 2.01922300298845e-5
allele num: 99048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+12A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+12A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+12A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+12A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.258+12A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.322+12A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+12A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+12A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+17A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+17A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.343+12A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+12A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.56+12A>G
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10666
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33013
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

7-73152653-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152653
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152653
    reference: chr 7
allele count: 2
allele frequency: 1.957828376764493e-5
allele num: 102154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.56+5G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+5G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+5G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+10G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+5G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+10G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+5G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+5G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+5G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.258+5G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.343+5G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.322+5G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+5G>A
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.288+5G>A
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

7-73152657-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152657
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152657
    reference: chr 7
allele count: 1
allele frequency: 9.670992824123324e-6
allele num: 103402
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.288+1G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.183+1G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.288+1G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.343+1G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.258+1G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.267+6G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.230+1G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.283+6G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.267+1G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.56+1G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.322+1G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.288+1G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.136+1G>A
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.288+1G>A
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

7-73152664-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152664
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152664
    reference: chr 7
allele count: 4
allele frequency: 3.789960394913873e-5
allele num: 105542
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.282C>G
  hgvsp: ENST00000222800.3:c.282C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.224C>G
  hgvsp: ENST00000412965.1:c.224C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.282C>G
  hgvsp: ENST00000458339.1:c.282C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.316C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.130C>G
  hgvsp: ENST00000437891.1:c.130C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.266C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.282C>G
  hgvsp: ENST00000395147.4:c.282C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.282C>G
  hgvsp: ENST00000357419.4:c.282C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.337C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.252C>G
  hgvsp: ENST00000474130.1:c.252C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.261C>G
  hgvsp: ENST00000437775.2:c.261C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.177C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.50C>G
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36787
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7648
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.266C>G
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

7-73152664-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152664
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152664
    reference: chr 7
allele count: 1
allele frequency: 9.474900987284683e-6
allele num: 105542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.282C>A
  hgvsp: ENST00000357419.4:c.282C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.224C>A
  hgvsp: ENST00000412965.1:c.224C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.282C>A
  hgvsp: ENST00000395147.4:c.282C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.337C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.50C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.130C>A
  hgvsp: ENST00000437891.1:c.130C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.316C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.282C>A
  hgvsp: ENST00000458339.1:c.282C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.252C>A
  hgvsp: ENST00000474130.1:c.252C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.261C>A
  hgvsp: ENST00000437775.2:c.261C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.266C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.177C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.282C>A
  hgvsp: ENST00000222800.3:c.282C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7648
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.266C>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

7-73152665-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152665
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152665
    reference: chr 7
allele count: 1
allele frequency: 9.457874626413952e-6
allele num: 105732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.315G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.265G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.281G>A
  hgvsp: ENSP00000222800.3:p.Gly94Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.176G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.129G>A
  hgvsp: ENSP00000410536.1:p.Gly44Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.336G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.260G>A
  hgvsp: ENSP00000416970.2:p.Gly87Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.281G>A
  hgvsp: ENSP00000392945.2:p.Gly94Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.251G>A
  hgvsp: ENSP00000430937.1:p.Gly84Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.49G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.281G>A
  hgvsp: ENSP00000378579.4:p.Gly94Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.281G>A
  hgvsp: ENSP00000397666.1:p.Gly94Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.223G>A
  hgvsp: ENSP00000387908.1:p.Gly75Asp
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7548
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly94Asp
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-73152666-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152666
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152666
    reference: chr 7
allele count: 2
allele frequency: 1.884623358021899e-5
allele num: 106122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.280G>T
  hgvsp: ENSP00000392945.2:p.Gly94Cys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.175G>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.280G>T
  hgvsp: ENSP00000378579.4:p.Gly94Cys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.280G>T
  hgvsp: ENSP00000397666.1:p.Gly94Cys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.250G>T
  hgvsp: ENSP00000430937.1:p.Gly84Cys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.314G>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.128G>T
  hgvsp: ENSP00000410536.1:p.Gly44Cys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.222G>T
  hgvsp: ENSP00000387908.1:p.Gly75Cys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.259G>T
  hgvsp: ENSP00000416970.2:p.Gly87Cys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.280G>T
  hgvsp: ENSP00000222800.3:p.Gly94Cys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.48G>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.335G>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.264G>T
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37210
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly94Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ

7-73152671-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152671
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152671
    reference: chr 7
allele count: 1
allele frequency: 9.300249246679811e-6
allele num: 107524
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.259A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.245A>G
  hgvsp: ENSP00000430937.1:p.Gln82Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.275A>G
  hgvsp: ENSP00000378579.4:p.Gln92Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.217A>G
  hgvsp: ENSP00000387908.1:p.Gln73Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.309A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.123A>G
  hgvsp: ENSP00000410536.1:p.Gln42Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.275A>G
  hgvsp: ENSP00000397666.1:p.Gln92Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.275A>G
  hgvsp: ENSP00000222800.3:p.Gln92Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.275A>G
  hgvsp: ENSP00000392945.2:p.Gln92Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.254A>G
  hgvsp: ENSP00000416970.2:p.Gln85Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.43A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.330A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.170A>G
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln92Arg
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP

7-73152673-CTGGGCCAAGAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152673
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152662
    reference: chr 7
allele count: 1
allele frequency: 9.290054068114676e-6
allele num: 107642
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.30_40delATCTTGGCCCA
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsp: ENSP00000387908.1:p.Ile69AlafsTer5
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsp: ENSP00000222800.3:p.Ile88AlafsTer5
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsp: ENSP00000416970.2:p.Ile81AlafsTer5
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsp: ENSP00000410536.1:p.Ile38AlafsTer5
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsp: ENSP00000392945.2:p.Ile88AlafsTer6
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsp: ENSP00000397666.1:p.Ile88AlafsTer5
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsp: ENSP00000430937.1:p.Ile78AlafsTer5
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsp: ENSP00000378579.4:p.Ile88AlafsTer5
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9185
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile88AlafsTer5
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: CTGGGCCAAGAT
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

7-73152685-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152685
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152685
    reference: chr 7
allele count: 2
allele frequency: 1.852229157791402e-5
allele num: 107978
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.261G>A
  hgvsp: ENST00000357419.4:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.29G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.261G>A
  hgvsp: ENST00000395147.4:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.109G>A
  hgvsp: ENST00000437891.1:c.109G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.295G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.240G>A
  hgvsp: ENST00000437775.2:c.240G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.156G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.261G>A
  hgvsp: ENST00000458339.1:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.261G>A
  hgvsp: ENST00000222800.3:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.231G>A
  hgvsp: ENST00000474130.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.203G>A
  hgvsp: ENST00000412965.1:c.203G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.245G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.316G>A
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9807
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys87Lys
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-73152687-TGGC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152687
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152684
    reference: chr 7
allele count: 1
allele frequency: 9.274201027581474e-6
allele num: 107826
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.256_258delGCC
  hgvsp: ENSP00000222800.3:p.Ala86del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.235_237delGCC
  hgvsp: ENSP00000416970.2:p.Ala79del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.151_153delGCC
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.104_106delGCC
  hgvsp: ENSP00000410536.1:p.Ala36del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.311_313delGCC
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.290_292delGCC
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.256_258delGCC
  hgvsp: ENSP00000378579.4:p.Ala86del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.256_258delGCC
  hgvsp: ENSP00000397666.1:p.Ala86del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.198_200delGCC
  hgvsp: ENSP00000387908.1:p.Ala67del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.256_258delGCC
  hgvsp: ENSP00000392945.2:p.Ala86del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.240_242delGCC
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.226_228delGCC
  hgvsp: ENSP00000430937.1:p.Ala76del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.24_26delGCC
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35826
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala86del
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: TGGC
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

7-73152689-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152689
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152689
    reference: chr 7
allele count: 1
allele frequency: 9.290054068114676e-6
allele num: 107642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.257C>T
  hgvsp: ENSP00000378579.4:p.Ala86Val
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.291C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.312C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.105C>T
  hgvsp: ENSP00000410536.1:p.Ala36Val
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.199C>T
  hgvsp: ENSP00000387908.1:p.Ala67Val
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.236C>T
  hgvsp: ENSP00000416970.2:p.Ala79Val
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.227C>T
  hgvsp: ENSP00000430937.1:p.Ala76Val
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.257C>T
  hgvsp: ENSP00000397666.1:p.Ala86Val
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.257C>T
  hgvsp: ENSP00000392945.2:p.Ala86Val
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.257C>T
  hgvsp: ENSP00000222800.3:p.Ala86Val
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.152C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.241C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.25C>T
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala86Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP

7-73152692-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152692
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152692
    reference: chr 7
allele count: 1
allele frequency: 9.311333755447131e-6
allele num: 107396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.224T>C
  hgvsp: ENSP00000430937.1:p.Ile75Thr
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.238T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.254T>C
  hgvsp: ENSP00000397666.1:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.196T>C
  hgvsp: ENSP00000387908.1:p.Ile66Thr
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.233T>C
  hgvsp: ENSP00000416970.2:p.Ile78Thr
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.254T>C
  hgvsp: ENSP00000222800.3:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.254T>C
  hgvsp: ENSP00000378579.4:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.288T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.309T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.22T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.102T>C
  hgvsp: ENSP00000410536.1:p.Ile35Thr
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.254T>C
  hgvsp: ENSP00000392945.2:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.149T>C
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34442
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile85Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-73152694-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152694
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152694
    reference: chr 7
allele count: 48
allele frequency: 4.471605306304964e-4
allele num: 107344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.222C>T
  hgvsp: ENST00000474130.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.307C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.252C>T
  hgvsp: ENST00000458339.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.252C>T
  hgvsp: ENST00000357419.4:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.20C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.194C>T
  hgvsp: ENST00000412965.1:c.194C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.231C>T
  hgvsp: ENST00000437775.2:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.147C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.252C>T
  hgvsp: ENST00000222800.3:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.252C>T
  hgvsp: ENST00000395147.4:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.286C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.100C>T
  hgvsp: ENST00000437891.1:c.100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.236C>T
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 34216
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10029
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser84Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum

7-73152694-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152694
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152694
    reference: chr 7
allele count: 1
allele frequency: 9.31584438813534e-6
allele num: 107344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.252C>A
  hgvsp: ENST00000458339.1:c.252C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.252C>A
  hgvsp: ENST00000395147.4:c.252C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.194C>A
  hgvsp: ENST00000412965.1:c.194C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.231C>A
  hgvsp: ENST00000437775.2:c.231C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.222C>A
  hgvsp: ENST00000474130.1:c.222C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.307C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.147C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.20C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.252C>A
  hgvsp: ENST00000222800.3:c.252C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.252C>A
  hgvsp: ENST00000357419.4:c.252C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.236C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.100C>A
  hgvsp: ENST00000437891.1:c.100C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.286C>A
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10029
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser84Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

7-73152698-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152698
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152698
    reference: chr 7
allele count: 1
allele frequency: 9.362243942628168e-6
allele num: 106812
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.248A>G
  hgvsp: ENSP00000378579.4:p.Asn83Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.232A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.282A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.248A>G
  hgvsp: ENSP00000392945.2:p.Asn83Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.248A>G
  hgvsp: ENSP00000222800.3:p.Asn83Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.16A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.218A>G
  hgvsp: ENSP00000430937.1:p.Asn73Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.143A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.227A>G
  hgvsp: ENSP00000416970.2:p.Asn76Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.248A>G
  hgvsp: ENSP00000397666.1:p.Asn83Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.96A>G
  hgvsp: ENSP00000410536.1:p.Asn33Ser
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.303A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.190A>G
  hgvsp: ENSP00000387908.1:p.Asn64Ser
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5969
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn83Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

7-73152703-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152703
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152703
    reference: chr 7
allele count: 2
allele frequency: 1.882955486932289e-5
allele num: 106216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.185C>G
  hgvsp: ENSP00000387908.1:p.Asn62Lys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.277C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.138C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.243C>G
  hgvsp: ENSP00000222800.3:p.Asn81Lys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.243C>G
  hgvsp: ENSP00000392945.2:p.Asn81Lys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.298C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.243C>G
  hgvsp: ENSP00000378579.4:p.Asn81Lys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.243C>G
  hgvsp: ENSP00000397666.1:p.Asn81Lys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.11C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.222C>G
  hgvsp: ENSP00000416970.2:p.Asn74Lys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.213C>G
  hgvsp: ENSP00000430937.1:p.Asn71Lys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.91C>G
  hgvsp: ENSP00000410536.1:p.Asn31Lys
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.227C>G
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6643
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn81Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

7-73152705-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152705
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152705
    reference: chr 7
allele count: 40
allele frequency: 3.775935960126116e-4
allele num: 105934
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.89A>G
  hgvsp: ENSP00000410536.1:p.Asn31Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.211A>G
  hgvsp: ENSP00000430937.1:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.241A>G
  hgvsp: ENSP00000397666.1:p.Asn81Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.220A>G
  hgvsp: ENSP00000416970.2:p.Asn74Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.225A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.241A>G
  hgvsp: ENSP00000392945.2:p.Asn81Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468331
  gene symbol: ABHD11
  hgvsc: ENST00000468331.1:n.9A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.136A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.241A>G
  hgvsp: ENSP00000378579.4:p.Asn81Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.183A>G
  hgvsp: ENSP00000387908.1:p.Asn62Asp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.275A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.296A>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.241A>G
  hgvsp: ENSP00000222800.3:p.Asn81Asp
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7010
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn81Asp
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

7-73152718-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152718
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152718
    reference: chr 7
allele count: 2
allele frequency: 1.938698357922491e-5
allele num: 103162
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.228C>G
  hgvsp: ENSP00000392945.2:p.Phe76Leu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.228C>G
  hgvsp: ENSP00000378579.4:p.Phe76Leu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.228C>G
  hgvsp: ENSP00000397666.1:p.Phe76Leu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.262C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.207C>G
  hgvsp: ENSP00000416970.2:p.Phe69Leu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.198C>G
  hgvsp: ENSP00000430937.1:p.Phe66Leu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.170C>G
  hgvsp: ENSP00000387908.1:p.Phe57Leu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.228C>G
  hgvsp: ENSP00000222800.3:p.Phe76Leu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.212C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.76C>G
  hgvsp: ENSP00000410536.1:p.Phe26Leu
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.283C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.123C>G
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9206
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26511
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe76Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/7-73152726-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152726
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152726
    reference: chr 7
allele count: 1
allele frequency: 9.878689690599439e-6
allele num: 101228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.220G>T
  hgvsp: ENSP00000392945.2:p.Gly74Trp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.199G>T
  hgvsp: ENSP00000416970.2:p.Gly67Trp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.220G>T
  hgvsp: ENSP00000222800.3:p.Gly74Trp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.220G>T
  hgvsp: ENSP00000378579.4:p.Gly74Trp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.162G>T
  hgvsp: ENSP00000387908.1:p.Gly55Trp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.68G>T
  hgvsp: ENSP00000410536.1:p.Gly24Trp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.190G>T
  hgvsp: ENSP00000430937.1:p.Gly64Trp
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.275G>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.254G>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.204G>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.115G>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.220G>T
  hgvsp: ENSP00000397666.1:p.Gly74Trp
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5051
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24167
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly74Trp
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

7-73152727-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152727
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152727
    reference: chr 7
allele count: 1
allele frequency: 9.902754946426096e-6
allele num: 100982
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.219C>A
  hgvsp: ENSP00000392945.2:p.His73Gln
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.198C>A
  hgvsp: ENSP00000416970.2:p.His66Gln
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.253C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.67C>A
  hgvsp: ENSP00000410536.1:p.His23Gln
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.219C>A
  hgvsp: ENSP00000397666.1:p.His73Gln
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.161C>A
  hgvsp: ENSP00000387908.1:p.His54Gln
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.219C>A
  hgvsp: ENSP00000222800.3:p.His73Gln
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.189C>A
  hgvsp: ENSP00000430937.1:p.His63Gln
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.203C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.114C>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.219C>A
  hgvsp: ENSP00000378579.4:p.His73Gln
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.274C>A
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His73Gln
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS

7-73152733-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152733
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152733
    reference: chr 7
allele count: 1
allele frequency: 1.013581998783702e-5
allele num: 98660
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.197T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.192T>C
  hgvsp: ENST00000437775.2:c.192T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.61T>C
  hgvsp: ENST00000437891.1:c.61T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.213T>C
  hgvsp: ENST00000395147.4:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.213T>C
  hgvsp: ENST00000222800.3:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.213T>C
  hgvsp: ENST00000357419.4:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.183T>C
  hgvsp: ENST00000474130.1:c.183T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.247T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.108T>C
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.155T>C
  hgvsp: ENST00000412965.1:c.155T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.213T>C
  hgvsp: ENST00000458339.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.268T>C
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6744
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19717
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Phe71Phe
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

7-73152740-ACGGCCGGGAGGG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152740
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152728
    reference: chr 7
allele count: 1
allele frequency: 1.044386422976501e-5
allele num: 95750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsp: ENSP00000430937.1:p.Ala55_Ala58del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsp: ENSP00000416970.2:p.Ala58_Ala61del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsp: ENSP00000387908.1:p.Ala46_Ala49del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsp: ENSP00000410536.1:p.Ala15_Ala18del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsp: ENSP00000222800.3:p.Ala65_Ala68del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsp: ENSP00000378579.4:p.Ala65_Ala68del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsp: ENSP00000397666.1:p.Ala65_Ala68del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsp: ENSP00000392945.2:p.Ala65_Ala68del
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14106
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8043
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala65_Ala68del
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: ACGGCCGGGAGGG
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

7-73152745-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152745
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152745
    reference: chr 7
allele count: 1
allele frequency: 1.065984436627225e-5
allele num: 93810
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.49G>A
  hgvsp: ENST00000437891.1:c.49G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.256G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.185G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.171G>A
  hgvsp: ENST00000474130.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.96G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.143G>A
  hgvsp: ENST00000412965.1:c.143G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.201G>A
  hgvsp: ENST00000222800.3:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.235G>A
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.201G>A
  hgvsp: ENST00000357419.4:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.201G>A
  hgvsp: ENST00000458339.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.180G>A
  hgvsp: ENST00000437775.2:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.201G>A
  hgvsp: ENST00000395147.4:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5925
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro67Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

7-73152746-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152746
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152746
    reference: chr 7
allele count: 1
allele frequency: 1.068033749866496e-5
allele num: 93630
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.170C>G
  hgvsp: ENSP00000430937.1:p.Pro57Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.179C>G
  hgvsp: ENSP00000416970.2:p.Pro60Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.48C>G
  hgvsp: ENSP00000410536.1:p.Pro17Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.142C>G
  hgvsp: ENSP00000387908.1:p.Pro48Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.184C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.200C>G
  hgvsp: ENSP00000378579.4:p.Pro67Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.95C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.234C>G
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.200C>G
  hgvsp: ENSP00000397666.1:p.Pro67Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.200C>G
  hgvsp: ENSP00000222800.3:p.Pro67Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.200C>G
  hgvsp: ENSP00000392945.2:p.Pro67Arg
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.255C>G
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8066
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro67Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

7-73152751-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73152751
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73152751
    reference: chr 7
allele count: 12
allele frequency: 1.290877796901893e-4
allele num: 92960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000397666
  ensembl transcript: ENST00000458339
  gene symbol: ABHD11
  hgvsc: ENST00000458339.1:c.195C>T
  hgvsp: ENST00000458339.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000497897
  gene symbol: ABHD11
  hgvsc: ENST00000497897.1:n.179C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000410536
  ensembl transcript: ENST00000437891
  gene symbol: ABHD11
  hgvsc: ENST00000437891.1:c.43C>T
  hgvsp: ENST00000437891.1:c.43C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000387908
  ensembl transcript: ENST00000412965
  gene symbol: ABHD11
  hgvsc: ENST00000412965.1:c.137C>T
  hgvsp: ENST00000412965.1:c.137C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000392945
  ensembl transcript: ENST00000357419
  gene symbol: ABHD11
  hgvsc: ENST00000357419.4:c.195C>T
  hgvsp: ENST00000357419.4:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000430937
  ensembl transcript: ENST00000474130
  gene symbol: ABHD11
  hgvsc: ENST00000474130.1:c.165C>T
  hgvsp: ENST00000474130.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000416970
  ensembl transcript: ENST00000437775
  gene symbol: ABHD11
  hgvsc: ENST00000437775.2:c.174C>T
  hgvsp: ENST00000437775.2:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000222800
  ensembl transcript: ENST00000222800
  gene symbol: ABHD11
  hgvsc: ENST00000222800.3:c.195C>T
  hgvsp: ENST00000222800.3:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000486114
  gene symbol: ABHD11
  hgvsc: ENST00000486114.1:n.90C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000480445
  gene symbol: ABHD11
  hgvsc: ENST00000480445.1:n.250C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106077
  ensembl transcript: ENST00000468998
  gene symbol: ABHD11
  hgvsc: ENST00000468998.1:n.229C>T
  variant of: http://identifiers.org/hgnc/16407
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106077
  ensembl protein: ENSP00000378579
  ensembl transcript: ENST00000395147
  gene symbol: ABHD11
  hgvsc: ENST00000395147.4:c.195C>T
  hgvsp: ENST00000395147.4:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16407
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17297
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12779
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14569
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala65Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 517
bin: 4.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1357
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1748
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5636
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1085
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 149
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46620
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15774
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6206
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.083202131524766e-5
allele num: 66056
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.514645e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

FS
type: SiteQuality
SIO_000300: 3.256e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.229e0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.112e1

GenotypeDepth
all individuals: 126
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2056
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5599
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46094
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 148
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 2.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15584
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.738828029907842e-4
allele num: 11502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.579662250250129e-5
allele num: 65966
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.509142e6

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.254e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

QD
type: SiteQuality
SIO_000300: 1.062e1

GenotypeDepth
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2393
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1353
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45572
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5547
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1490
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65842
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6178
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15360
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.023e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 8.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.02e-1

MQ
type: SiteQuality
SIO_000300: 5.794e1

FS
type: SiteQuality
SIO_000300: 3.866e0

MQRankSum
type: SiteQuality
SIO_000300: 2.54e0

DP
type: SiteQuality
SIO_000300: 1.50281e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.225e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.19e0

GenotypeDepth
all individuals: 127
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 6.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6170
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.710623422023694e-5
allele num: 10298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.080690766471071e-5
allele num: 65782
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

Other
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allele count: 0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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DP
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.524250830716703e-5
allele num: 65606
num of homozygotes: 0

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

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

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6118
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65424
num of homozygotes: 0

African
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allele count: 1
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allele num: 10254
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Other
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FS
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SIO_000300: 2.4859e1

MQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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ClippingRankSum
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MQ
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BaseQRankSum
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SIO_000300: -2.01e-1

QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.53261402648357e-5
allele num: 65248
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
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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Latino
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European (Non-Finnish)
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allele num: 65182
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Other
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QD
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FS
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MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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Other
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East Asian
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Latino
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DP
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FS
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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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ClippingRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 8366
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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African
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allele frequency: 4.136504653567735e-4
allele num: 9670
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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MQ
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.044495508669313e-4
allele num: 9574
num of homozygotes: 0

Other
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South Asian
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Latino
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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MQRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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DP
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FS
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10578
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 num: 9578
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10412
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61448
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European (Finnish)
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allele frequency: 0.0e0
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Other
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MQRankSum
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BaseQRankSum
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QD
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DP
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.19019281123542e-4
allele num: 8402
num of homozygotes: 0

East Asian
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European (Finnish)
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African
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allele num: 2098
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Latino
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South Asian
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Other
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FS
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MQ
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ClippingRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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Other
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African
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European (Non-Finnish)
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VQSLOD
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ClippingRankSum
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MQRankSum
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QD
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MQ
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DP
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BaseQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 7904
num of homozygotes: 0

European (Non-Finnish)
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Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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African
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FS
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MQ
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ClippingRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQRankSum
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QD
type: SiteQuality
SIO_000300: 1.122e1

GenotypeDepth
all individuals: 240
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 784
bin: 6.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2591
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
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GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2042
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.211827435773146e-4
allele num: 8252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.13e0

DP
type: SiteQuality
SIO_000300: 5.2856e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.716e0

QD
type: SiteQuality
SIO_000300: 1.339e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.425e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-2

FS
type: SiteQuality
SIO_000300: 1.69343e2

MQ
type: SiteQuality
SIO_000300: 6.003e1

MQRankSum
type: SiteQuality
SIO_000300: 2.76e0

VQSLOD
type: SiteQuality
SIO_000300: -1.428e2

GenotypeDepth
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bin: 6.25e1
variant carriers: 4

GenotypeDepth
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variant carriers: 10

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
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bin: 9.75e1
variant carriers: 38

GenotypeQuality
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bin: 5.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.590673575129534e-3
allele num: 386
num of homozygotes: 0

African
type: Population
allele count: 36
allele frequency: 1.725790987535954e-2
allele num: 2086
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.265502404454569e-4
allele num: 7902
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.432e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.54e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.356e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.86e0

FS
type: SiteQuality
SIO_000300: 1.763e0

DP
type: SiteQuality
SIO_000300: 5.26215e5

GenotypeDepth
all individuals: 435
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variant carriers: 0

GenotypeDepth
all individuals: 764
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 358
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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: 0

GenotypeQuality
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bin: 2.5e0
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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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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 186
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GenotypeQuality
all individuals: 264
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 9.587727708533077e-4
allele num: 2086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.73e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.16e-1

QD
type: SiteQuality
SIO_000300: 1.232e1

VQSLOD
type: SiteQuality
SIO_000300: -4.237e-1

FS
type: SiteQuality
SIO_000300: 1.179e0

DP
type: SiteQuality
SIO_000300: 5.25124e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 710
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variant carriers: 0

GenotypeDepth
all individuals: 435
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variant carriers: 0

GenotypeDepth
all individuals: 357
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variant carriers: 0

GenotypeDepth
all individuals: 157
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variant carriers: 0

GenotypeQuality
all individuals: 86
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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: 31
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variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6708
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3338
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
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variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2078
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.266464032421479e-4
allele num: 7896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.8e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.77e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.27e0

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

DP
type: SiteQuality
SIO_000300: 5.24191e5

VQSLOD
type: SiteQuality
SIO_000300: -1.796e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

GenotypeDepth
all individuals: 359
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 711
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variant carriers: 1

GenotypeDepth
all individuals: 765
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 435
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variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4610
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 180
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variant carriers: 0

GenotypeQuality
all individuals: 180
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variant carriers: 0

GenotypeQuality
all individuals: 189
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variant carriers: 0

GenotypeQuality
all individuals: 218
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variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

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: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8288
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 6.711409395973154e-3
allele num: 596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7888
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.82e-1

MQ
type: SiteQuality
SIO_000300: 5.929e1

FS
type: SiteQuality
SIO_000300: 2.862e0

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

BaseQRankSum
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SIO_000300: -1.881e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.899999999999999e-1

DP
type: SiteQuality
SIO_000300: 5.24043e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.85e-2

QD
type: SiteQuality
SIO_000300: 1.218e1

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2074
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8286
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.80420999239158e-4
allele num: 7886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

FS
type: SiteQuality
SIO_000300: 2.538e0

VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.232e1

BaseQRankSum
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SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.07e-2

DP
type: SiteQuality
SIO_000300: 5.24638e5

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

GenotypeDepth
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variant carriers: 0

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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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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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GenotypeQuality
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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: 6013
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GenotypeQuality
all individuals: 6663
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3464
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11094
num of homozygotes: 0

East 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: 8252
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.073054438409553e-5
allele num: 48238
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6854
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

QD
type: SiteQuality
SIO_000300: 1.174e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 8.36063e5

BaseQRankSum
type: SiteQuality
SIO_000300: 5.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.33e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1413
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 9.75e1
variant carriers: 5

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8252
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 7.348618459729571e-4
allele num: 6804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.073054438409553e-5
allele num: 48238
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11094
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.174e1

DP
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SIO_000300: 8.36063e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47824
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.043226623259179e-5
allele num: 11058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3358
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.224289911851126e-4
allele num: 8168
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.469723691945914e-4
allele num: 6804
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.382e0

MQRankSum
type: SiteQuality
SIO_000300: -7.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

DP
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SIO_000300: 8.64695e5

BaseQRankSum
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SIO_000300: 2.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

QD
type: SiteQuality
SIO_000300: 1.482e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.64e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 143
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6966
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6940
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.029962242702286e-5
allele num: 49262
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.79359e5

ClippingRankSum
type: SiteQuality
SIO_000300: 6.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.01e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

MQ
type: SiteQuality
SIO_000300: 5.929e1

QD
type: SiteQuality
SIO_000300: 1.754e1

FS
type: SiteQuality
SIO_000300: 2.946e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.984e0

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.69e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 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
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.015072744126063e-5
allele num: 49626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3670
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7008
num of homozygotes: 0

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

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

African
type: Population
allele count: 4
allele frequency: 5.691519635742744e-4
allele num: 7028
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.162000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

MQ
type: SiteQuality
SIO_000300: 6.06e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.296e0

VQSLOD
type: SiteQuality
SIO_000300: 3.66e-1

DP
type: SiteQuality
SIO_000300: 9.00579e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 70
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.418439716312057e-4
allele num: 7050
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3674
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 49826
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.766e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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MQRankSum
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SIO_000300: -1.03e-1

ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -5.3e-3

VQSLOD
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DP
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SIO_000300: 9.19712e5

ClippingRankSum
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SIO_000300: 3.82e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 634
num of homozygotes: 0

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

African
type: Population
allele count: 9
allele frequency: 1.27262443438914e-3
allele num: 7072
num of homozygotes: 0

European (Finnish)
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
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num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50160
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

VQSLOD
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ReadPosRankSum
type: SiteQuality
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MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
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MQRankSum
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SIO_000300: 9.1e-2

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 422
bin: 9.75e1
variant carriers: 17

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7072
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 1.80940892641737e-3
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East Asian
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Latino
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Other
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European (Non-Finnish)
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ClippingRankSum
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ReadPosRankSum
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QD
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MQ
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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East Asian
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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FS
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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VQSLOD
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MQRankSum
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ClippingRankSum
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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Latino
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European (Finnish)
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European (Non-Finnish)
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South Asian
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Other
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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QD
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MQ
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FS
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 54050
num of homozygotes: 0

East Asian
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South Asian
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Latino
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African
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allele num: 7706
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European (Finnish)
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Other
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ClippingRankSum
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VQSLOD
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MQ
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DP
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FS
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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South Asian
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MQRankSum
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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East Asian
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Other
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African
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Latino
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South Asian
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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FS
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DP
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InbreedingCoeff
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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Latino
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European (Non-Finnish)
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South Asian
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African
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East Asian
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DP
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QD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 3.957261574990107e-4
allele num: 10108
num of homozygotes: 0

European (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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South Asian
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European (Non-Finnish)
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FS
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MQRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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ClippingRankSum
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DP
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VQSLOD
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58772
num of homozygotes: 0

Other
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South Asian
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allele frequency: 6.875687568756875e-5
allele num: 14544
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African
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East Asian
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Latino
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European (Finnish)
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FS
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MQRankSum
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DP
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BaseQRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 58864
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African
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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South Asian
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MQ
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FS
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DP
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.25e1
variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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East Asian
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Other
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European (Non-Finnish)
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allele frequency: 3.385354954466976e-5
allele num: 59078
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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QD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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FS
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MQ
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GenotypeDepth
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variant carriers: 0

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

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

South Asian
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East Asian
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African
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Other
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Latino
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European (Finnish)
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MQRankSum
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BaseQRankSum
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DP
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QD
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FS
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MQ
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Latino
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Other
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European (Non-Finnish)
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InbreedingCoeff
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BaseQRankSum
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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DP
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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African
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Other
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European (Non-Finnish)
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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QD
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ReadPosRankSum
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DP
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MQ
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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South Asian
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East Asian
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Latino
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European (Finnish)
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QD
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ClippingRankSum
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DP
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BaseQRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.377579626439694e-5
allele num: 59214
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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ClippingRankSum
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FS
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DP
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QD
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MQ
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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South Asian
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allele num: 14826
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Latino
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European (Finnish)
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MQ
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QD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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allele num: 57590
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South Asian
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Latino
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African
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European (Finnish)
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FS
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InbreedingCoeff
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DP
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
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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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East Asian
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South Asian
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European (Non-Finnish)
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allele num: 56486
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Other
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DP
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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QD
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FS
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Other
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Latino
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European (Non-Finnish)
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European (Finnish)
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South Asian
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ClippingRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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BaseQRankSum
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DP
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VQSLOD
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MQ
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MQRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Latino
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South Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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FS
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QD
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BaseQRankSum
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MQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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African
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South Asian
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InbreedingCoeff
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QD
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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DP
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MQRankSum
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FS
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MQ
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BaseQRankSum
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SIO_000300: 1.93e0

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 163
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1384
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18996
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18378
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2015
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4105
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3971
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3052
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1685
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 97
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 7.5e0
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14062
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3998
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.426533523537803e-4
allele num: 7010
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e0

QD
type: SiteQuality
SIO_000300: 1.014e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.108e0

MQRankSum
type: SiteQuality
SIO_000300: -4.65e-1

DP
type: SiteQuality
SIO_000300: 1.005216e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.58e-1

FS
type: SiteQuality
SIO_000300: 1.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.69e-1

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

GenotypeDepth
all individuals: 8
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2994
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1617
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3965
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4091
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14052
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6980
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.921820348233847e-5
allele num: 52034
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7392
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4014
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
SIO_000300: 2.741e0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.156e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

QD
type: SiteQuality
SIO_000300: 7.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

DP
type: SiteQuality
SIO_000300: 1.003823e6

MQ
type: SiteQuality
SIO_000300: 5.827e1

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

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

GenotypeDepth
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4128
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1383
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 4031
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19883
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1801
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2977
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18741
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 2.319916483006612e-4
allele num: 51726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6954
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3944
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13980
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

FS
type: SiteQuality
SIO_000300: 4.155e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.0e-2