11-134130933-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130933
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130933
    reference: chr 11
allele count: 5
allele frequency: 4.91651753230152e-5
allele num: 101698
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*395-5G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.562-5G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1094-5G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.706-5G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*305-5G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.412-5G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.309-5G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.332-5G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.325-5G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1760G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.475-5G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20632
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.706-5G>A
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

11-134130937-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130937
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130937
    reference: chr 11
allele count: 5
allele frequency: 4.878715141580313e-5
allele num: 102486
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.412-1G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.475-1G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1094-1G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.332-1G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.562-1G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*395-1G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.325-1G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*305-1G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1764G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.309-1G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.706-1G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8932
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4129
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11425
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21054
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2507
  bin: 6.75e1
  variant carriers: 0
hgvs: c.706-1G>A
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

11-134130945-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130945
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130945
    reference: chr 11
allele count: 1
allele frequency: 9.670431688070555e-6
allele num: 103408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*402G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.316G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.482G>A
  hgvsp: ENSP00000443763.1:p.Trp161Ter
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.419G>A
  hgvsp: ENSP00000438302.1:p.Trp140Ter
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1101G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.713G>A
  hgvsp: ENSP00000281182.4:p.Trp238Ter
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.339G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.332G>A
  hgvsp: ENSP00000363884.4:p.Trp111Ter
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.569G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*312G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1772G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21958
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp238Ter
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

11-134130947-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130947
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130947
    reference: chr 11
allele count: 1
allele frequency: 9.633540133328195e-6
allele num: 103804
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.421A>G
  hgvsp: ENSP00000438302.1:p.Asn141Asp
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*404A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.715A>G
  hgvsp: ENSP00000281182.4:p.Asn239Asp
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1774A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1103A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.334A>G
  hgvsp: ENSP00000363884.4:p.Asn112Asp
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.571A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.484A>G
  hgvsp: ENSP00000443763.1:p.Asn162Asp
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*314A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.318A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.341A>G
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn239Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-134130959-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130959
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130959
    reference: chr 11
allele count: 1
allele frequency: 9.56791304680623e-6
allele num: 104516
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*326A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1786A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.583A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.433A>G
  hgvsp: ENSP00000438302.1:p.Thr145Ala
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.353A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.346A>G
  hgvsp: ENSP00000363884.4:p.Thr116Ala
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.727A>G
  hgvsp: ENSP00000281182.4:p.Thr243Ala
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*416A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.330A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.496A>G
  hgvsp: ENSP00000443763.1:p.Thr166Ala
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1115A>G
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10914
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5066
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr243Ala
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

11-134130962-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130962
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130962
    reference: chr 11
allele count: 1
allele frequency: 9.566082497895462e-6
allele num: 104536
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*329C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.586C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.436C>G
  hgvsp: ENSP00000438302.1:p.Arg146Gly
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1789C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.349C>G
  hgvsp: ENSP00000363884.4:p.Arg117Gly
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.730C>G
  hgvsp: ENSP00000281182.4:p.Arg244Gly
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.499C>G
  hgvsp: ENSP00000443763.1:p.Arg167Gly
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.356C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1118C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*419C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.333C>G
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg244Gly
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

11-134130962-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130962
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130962
    reference: chr 11
allele count: 2
allele frequency: 1.913216499579092e-5
allele num: 104536
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1118C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.436C>T
  hgvsp: ENSP00000438302.1:p.Arg146Ter
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.333C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.730C>T
  hgvsp: ENSP00000281182.4:p.Arg244Ter
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.586C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1789C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.349C>T
  hgvsp: ENSP00000363884.4:p.Arg117Ter
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.499C>T
  hgvsp: ENSP00000443763.1:p.Arg167Ter
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.356C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*419C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*329C>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10981
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg244Ter
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

11-134130963-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130963
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130963
    reference: chr 11
allele count: 4
allele frequency: 3.826506208506323e-5
allele num: 104534
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.350G>A
  hgvsp: ENSP00000363884.4:p.Arg117Gln
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.334G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.587G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*420G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.500G>A
  hgvsp: ENSP00000443763.1:p.Arg167Gln
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.357G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1119G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.437G>A
  hgvsp: ENSP00000438302.1:p.Arg146Gln
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.731G>A
  hgvsp: ENSP00000281182.4:p.Arg244Gln
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*330G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1790G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19893
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5410
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10958
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg244Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP

11-134130966-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130966
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130966
    reference: chr 11
allele count: 10
allele frequency: 9.565167486082682e-5
allele num: 104546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*423C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.337C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1122C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1793C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.353C>T
  hgvsp: ENSP00000363884.4:p.Ala118Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.503C>T
  hgvsp: ENSP00000443763.1:p.Ala168Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.590C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.440C>T
  hgvsp: ENSP00000438302.1:p.Ala147Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.360C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.734C>T
  hgvsp: ENSP00000281182.4:p.Ala245Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*333C>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19002
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6144
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11245
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala245Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum

11-134130970-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130970
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130970
    reference: chr 11
allele count: 1
allele frequency: 9.551828219921294e-6
allele num: 104692
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.738G>T
  hgvsp: ENST00000281182.4:c.738G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*337G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.364G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.444G>T
  hgvsp: ENST00000543332.1:c.444G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1126G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.507G>T
  hgvsp: ENST00000537423.1:c.507G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.594G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.341G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.357G>T
  hgvsp: ENST00000374752.4:c.357G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1797G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*427G>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6644
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val246Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-134130976-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130976
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130976
    reference: chr 11
allele count: 6
allele frequency: 5.735698990516978e-5
allele num: 104608
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.513C>T
  hgvsp: ENST00000537423.1:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.347C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1132C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.600C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*433C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*343C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1803C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.370C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.450C>T
  hgvsp: ENST00000543332.1:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.744C>T
  hgvsp: ENST00000281182.4:c.744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.363C>T
  hgvsp: ENST00000374752.4:c.363C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18325
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11464
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6820
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe248Phe
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: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

11-134130981-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130981
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130981
    reference: chr 11
allele count: 1
allele frequency: 9.504438572813504e-6
allele num: 105214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.455A>G
  hgvsp: ENSP00000438302.1:p.Asp152Gly
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1137A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*348A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.749A>G
  hgvsp: ENSP00000281182.4:p.Asp250Gly
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.375A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.518A>G
  hgvsp: ENSP00000443763.1:p.Asp173Gly
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.605A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.368A>G
  hgvsp: ENSP00000363884.4:p.Asp123Gly
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*438A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1808A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.352A>G
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6905
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6634
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp250Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-134130990-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130990
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130990
    reference: chr 11
allele count: 2
allele frequency: 1.892935564473385e-5
allele num: 105656
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1146T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.361T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.527T>G
  hgvsp: ENSP00000443763.1:p.Val176Gly
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*357T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.614T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*447T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.464T>G
  hgvsp: ENSP00000438302.1:p.Val155Gly
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.377T>G
  hgvsp: ENSP00000363884.4:p.Val126Gly
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1817T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.384T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.758T>G
  hgvsp: ENSP00000281182.4:p.Val253Gly
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7520
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val253Gly
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

11-134130991-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130991
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130991
    reference: chr 11
allele count: 7
allele frequency: 6.628034693027308e-5
allele num: 105612
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*448C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1147C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*358C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.615C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.528C>T
  hgvsp: ENST00000537423.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.759C>T
  hgvsp: ENST00000281182.4:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.378C>T
  hgvsp: ENST00000374752.4:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1818C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.385C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.465C>T
  hgvsp: ENST00000543332.1:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.362C>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6796
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7588
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11536
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val253Val
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

11-134130994-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130994
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130994
    reference: chr 11
allele count: 6
allele frequency: 5.685802551030078e-5
allele num: 105526
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.468T>C
  hgvsp: ENST00000543332.1:c.468T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.618T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1821T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*361T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.381T>C
  hgvsp: ENST00000374752.4:c.381T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.762T>C
  hgvsp: ENST00000281182.4:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.365T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.531T>C
  hgvsp: ENST00000537423.1:c.531T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.388T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1150T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*451T>C
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17481
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11534
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7694
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro254Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-134130999-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134130999
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134130999
    reference: chr 11
allele count: 2
allele frequency: 1.889787587875123e-5
allele num: 105832
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.536C>A
  hgvsp: ENSP00000443763.1:p.Ala179Asp
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.393C>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.370C>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.623C>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.473C>A
  hgvsp: ENSP00000438302.1:p.Ala158Asp
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.386C>A
  hgvsp: ENSP00000363884.4:p.Ala129Asp
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1826C>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*366C>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1155C>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.767C>A
  hgvsp: ENSP00000281182.4:p.Ala256Asp
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*456C>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11457
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7720
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala256Asp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS

11-134131007-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131007
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131007
    reference: chr 11
allele count: 1
allele frequency: 9.406983744732089e-6
allele num: 106304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.401A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1163A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.631A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.544A>G
  hgvsp: ENSP00000443763.1:p.Ile182Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.481A>G
  hgvsp: ENSP00000438302.1:p.Ile161Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*374A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.394A>G
  hgvsp: ENSP00000363884.4:p.Ile132Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*464A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1834A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.775A>G
  hgvsp: ENSP00000281182.4:p.Ile259Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.378A>G
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6934
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile259Val
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

11-134131015-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131015
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131015
    reference: chr 11
allele count: 2
allele frequency: 1.884836490434455e-5
allele num: 106110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.489C>T
  hgvsp: ENST00000543332.1:c.489C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.783C>T
  hgvsp: ENST00000281182.4:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.402C>T
  hgvsp: ENST00000374752.4:c.402C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.409C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.639C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.552C>T
  hgvsp: ENST00000537423.1:c.552C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*382C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1171C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*472C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1842C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.386C>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7322
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6757
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11039
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser261Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

11-134131016-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131016
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131016
    reference: chr 11
allele count: 5
allele frequency: 4.689287790970308e-5
allele num: 106626
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.490G>A
  hgvsp: ENSP00000438302.1:p.Glu164Lys
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*473G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.640G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.553G>A
  hgvsp: ENSP00000443763.1:p.Glu185Lys
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.410G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.784G>A
  hgvsp: ENSP00000281182.4:p.Glu262Lys
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1843G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1172G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*383G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.403G>A
  hgvsp: ENSP00000363884.4:p.Glu135Lys
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.387G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7388
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17628
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu262Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

11-134131027-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131027
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131027
    reference: chr 11
allele count: 1
allele frequency: 9.287465636377146e-6
allele num: 107672
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.501C>T
  hgvsp: ENST00000543332.1:c.501C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.398C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1183C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*394C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.414C>T
  hgvsp: ENST00000374752.4:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1854C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.564C>T
  hgvsp: ENST00000537423.1:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.421C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.795C>T
  hgvsp: ENST00000281182.4:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.651C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*484C>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6817
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly265Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

11-134131033-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131033
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131033
    reference: chr 11
allele count: 224
allele frequency: 2.068099564221877e-3
allele num: 108312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.657C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.420C>T
  hgvsp: ENST00000374752.4:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.570C>T
  hgvsp: ENST00000537423.1:c.570C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*490C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*400C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1860C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.427C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.507C>T
  hgvsp: ENST00000543332.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.404C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1189C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.801C>T
  hgvsp: ENST00000281182.4:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8294
  bin: 2.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 6257
  bin: 1.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19709
  bin: 2.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 9634
  bin: 1.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 3.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
hgvs: p.Leu267Leu
num of homozygotes: 4
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

11-134131036-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131036
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131036
    reference: chr 11
allele count: 5
allele frequency: 4.597785706403796e-5
allele num: 108748
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1863T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.510T>C
  hgvsp: ENST00000543332.1:c.510T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.407T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.660T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.804T>C
  hgvsp: ENST00000281182.4:c.804T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.430T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.573T>C
  hgvsp: ENST00000537423.1:c.573T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*493T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.423T>C
  hgvsp: ENST00000374752.4:c.423T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1192T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*403T>C
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20280
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5866
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8431
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile268Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

11-134131036-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131036
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131036
    reference: chr 11
allele count: 1
allele frequency: 9.195571412807591e-6
allele num: 108748
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.407T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1863T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.573T>G
  hgvsp: ENSP00000443763.1:p.Ile191Met
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.660T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.423T>G
  hgvsp: ENSP00000363884.4:p.Ile141Met
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.804T>G
  hgvsp: ENSP00000281182.4:p.Ile268Met
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*493T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*403T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.510T>G
  hgvsp: ENSP00000438302.1:p.Ile170Met
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.430T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1192T>G
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5866
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20280
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile268Met
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

11-134131046-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131046
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131046
    reference: chr 11
allele count: 1
allele frequency: 9.102162673851307e-6
allele num: 109864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1873G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.433G>A
  hgvsp: ENSP00000363884.4:p.Gly145Arg
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1202G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*503G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.583G>A
  hgvsp: ENSP00000443763.1:p.Gly195Arg
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.814G>A
  hgvsp: ENSP00000281182.4:p.Gly272Arg
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.440G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.520G>A
  hgvsp: ENSP00000438302.1:p.Gly174Arg
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.670G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*413G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.417G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21278
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3062
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly272Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-134131054-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131054
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131054
    reference: chr 11
allele count: 3
allele frequency: 2.715177844148792e-5
allele num: 110490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.425C>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1881C>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.448C>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.678C>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.528C>A
  hgvsp: ENSP00000438302.1:p.Asn176Lys
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*511C>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*421C>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.441C>A
  hgvsp: ENSP00000363884.4:p.Asn147Lys
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1210C>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.591C>A
  hgvsp: ENSP00000443763.1:p.Asn197Lys
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.822C>A
  hgvsp: ENSP00000281182.4:p.Asn274Lys
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22166
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn274Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

11-134131055-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131055
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131055
    reference: chr 11
allele count: 1
allele frequency: 9.029834573430615e-6
allele num: 110744
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.823G>A
  hgvsp: ENSP00000281182.4:p.Gly275Arg
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*422G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1882G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.442G>A
  hgvsp: ENSP00000363884.4:p.Gly148Arg
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*512G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.529G>A
  hgvsp: ENSP00000438302.1:p.Gly177Arg
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.449G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.592G>A
  hgvsp: ENSP00000443763.1:p.Gly198Arg
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1211G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.426G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.679G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly275Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

11-134131057-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131057
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131057
    reference: chr 11
allele count: 2
allele frequency: 1.798464111648652e-5
allele num: 111206
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.594A>T
  hgvsp: ENST00000537423.1:c.594A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.444A>T
  hgvsp: ENST00000374752.4:c.444A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.451A>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*424A>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1213A>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1884A>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.531A>T
  hgvsp: ENST00000543332.1:c.531A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*514A>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.428A>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.681A>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.825A>T
  hgvsp: ENST00000281182.4:c.825A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22825
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly275Gly
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

11-134131070-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131070
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131070
    reference: chr 11
allele count: 1
allele frequency: 8.841732979664014e-6
allele num: 113100
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.838A>G
  hgvsp: ENSP00000281182.4:p.Ile280Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.464A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.607A>G
  hgvsp: ENSP00000443763.1:p.Ile203Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1226A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.694A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*527A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*437A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.544A>G
  hgvsp: ENSP00000438302.1:p.Ile182Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.441A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.457A>G
  hgvsp: ENSP00000363884.4:p.Ile153Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1897A>G
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5716
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3956
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile280Val
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

11-134131071-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131071
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131071
    reference: chr 11
allele count: 1
allele frequency: 8.834858818956073e-6
allele num: 113188
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.458T>C
  hgvsp: ENSP00000363884.4:p.Ile153Thr
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*438T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.608T>C
  hgvsp: ENSP00000443763.1:p.Ile203Thr
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527713
  gene symbol: ACAD8
  hgvsc: ENST00000527713.1:n.465T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1898T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.839T>C
  hgvsp: ENSP00000281182.4:p.Ile280Thr
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*528T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.442T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.545T>C
  hgvsp: ENSP00000438302.1:p.Ile182Thr
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1227T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.695T>C
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25598
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile280Thr
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/11-134131079-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131079
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131079
    reference: chr 11
allele count: 6
allele frequency: 5.247048535198951e-5
allele num: 114350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.444+6A>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.547+6A>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*530+6A>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1900+6A>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.697+6A>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.460+6A>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1229+6A>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*440+6A>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.841+6A>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.610+6A>C
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11632
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5305
  bin: 2.25e1
  variant carriers: 0
hgvs: c.841+6A>C
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ

11-134131080-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131080
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131080
    reference: chr 11
allele count: 1784
allele frequency: 1.556664688841576e-2
allele num: 114604
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.610+7T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.460+7T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*530+7T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.547+7T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1900+7T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.841+7T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1229+7T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*440+7T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.444+7T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.697+7T>C
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 1.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 3.25e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 3.75e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 5.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 7.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 1.75e1
  variant carriers: 169
genotype depth: GenotypeDepth
  all individuals: 11644
  bin: 2.75e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 4.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 6.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 8.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 9.75e1
  variant carriers: 212
genotype depth: GenotypeDepth
  all individuals: 26267
  bin: 2.25e1
  variant carriers: 206
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 6.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 5.25e1
  variant carriers: 4
hgvs: c.841+7T>C
num of homozygotes: 128
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

11-134131082-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131082
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131082
    reference: chr 11
allele count: 12
allele frequency: 1.046171014088436e-4
allele num: 114704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*440+9C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.547+9C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.841+9C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1900+9C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.444+9C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.460+9C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.697+9C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*530+9C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1229+9C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.610+9C>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11943
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26293
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1789
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS

11-134131083-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131083
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131083
    reference: chr 11
allele count: 1
allele frequency: 8.699585899711174e-6
allele num: 114948
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1900+10G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1229+10G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.460+10G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.841+10G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*440+10G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.610+10G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*530+10G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.697+10G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.547+10G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.444+10G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26360
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-134131088-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131088
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131088
    reference: chr 11
allele count: 2
allele frequency: 1.730163673483511e-5
allele num: 115596
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.444+15G>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.547+15G>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1900+15G>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.697+15G>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1229+15G>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*440+15G>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*530+15G>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.460+15G>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.841+15G>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.610+15G>C
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25855
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4305
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29309
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1039
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

11-134131091-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131091
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131091
    reference: chr 11
allele count: 1
allele frequency: 8.634982039237358e-6
allele num: 115808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1900+18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.697+18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1229+18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.460+18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.547+18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*530+18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.610+18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*440+18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.841+18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.444+18G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

11-134131096-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131096
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131096
    reference: chr 11
allele count: 4
allele frequency: 3.436248990601859e-5
allele num: 116406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1900+23A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.841+23A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.460+23A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*440+23A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.610+23A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.444+23A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.547+23A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1229+23A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.697+23A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*530+23A>G
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25664
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4540
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1347
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

11-134131100-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131100
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131100
    reference: chr 11
allele count: 9
allele frequency: 7.920304139678964e-5
allele num: 113632
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*440+27A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.841+27A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1229+27A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*530+27A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.547+27A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.697+27A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.460+27A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1900+27A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.610+27A>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.444+27A>G
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13326
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25880
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5434
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 7.5e0
  variant carriers: 2
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

11-134131103-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131103
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131103
    reference: chr 11
allele count: 6
allele frequency: 5.185825410544512e-5
allele num: 115700
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*440+30T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1229+30T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*530+30T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1900+30T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.547+30T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.841+30T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.610+30T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.444+30T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.460+30T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.697+30T>G
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25313
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13429
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1435
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3277
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

11-134131107-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131107
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131107
    reference: chr 11
allele count: 5
allele frequency: 4.254667370105005e-5
allele num: 117518
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.547+34G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.841+34G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.697+34G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1229+34G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.444+34G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*530+34G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.460+34G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*440+34G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1900+34G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.610+34G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25953
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

11-134131107-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131107
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131107
    reference: chr 11
allele count: 1
allele frequency: 8.50933474021001e-6
allele num: 117518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.610+34G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1229+34G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.697+34G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1900+34G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.444+34G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*530+34G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.547+34G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*440+34G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.460+34G>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.841+34G>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14437
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

11-134131111-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131111
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131111
    reference: chr 11
allele count: 187
allele frequency: 1.584316117663007e-3
allele num: 118032
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1229+38C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.547+38C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.460+38C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.841+38C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1900+38C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*440+38C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.697+38C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*530+38C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.610+38C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.444+38C>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 26264
  bin: 2.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 14935
  bin: 2.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2216
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

11-134131112-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131112
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131112
    reference: chr 11
allele count: 2
allele frequency: 1.691246110133947e-5
allele num: 118256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.444+39G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.460+39G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*530+39G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.841+39G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1229+39G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.547+39G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*440+39G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.610+39G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1900+39G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.697+39G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5410
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1317
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33652
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

11-134131114-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131114
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131114
    reference: chr 11
allele count: 2
allele frequency: 1.68503353216729e-5
allele num: 118692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.610+41G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1229+41G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1900+41G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.841+41G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*440+41G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.547+41G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.460+41G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.444+41G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*530+41G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.697+41G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7223
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

11-134131123-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131123
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131123
    reference: chr 11
allele count: 1
allele frequency: 8.351149118118652e-6
allele num: 119744
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.461-46T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*531-46T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1901-46T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.548-46T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*441-46T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.698-46T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1230-46T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.611-46T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.445-46T>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.842-46T>G
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27720
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

11-134131128-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131128
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131128
    reference: chr 11
allele count: 1
allele frequency: 8.329862557267805e-6
allele num: 120050
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.611-41T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.548-41T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1901-41T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1230-41T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*441-41T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*531-41T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.445-41T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.698-41T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.461-41T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.842-41T>C
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: T
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

11-134131147-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131147
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131147
    reference: chr 11
allele count: 6
allele frequency: 4.968779502128294e-5
allele num: 120754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1230-22C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.445-22C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1901-22C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.611-22C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.548-22C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*531-22C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*441-22C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.461-22C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.842-22C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.698-22C>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7245
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2423
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

11-134131148-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131148
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131148
    reference: chr 11
allele count: 3
allele frequency: 2.482334055968359e-5
allele num: 120854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.445-21G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.611-21G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.698-21G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.548-21G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1230-21G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1901-21G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.842-21G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*531-21G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*441-21G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.461-21G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6159
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7210
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-134131151-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131151
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131151
    reference: chr 11
allele count: 10
allele frequency: 8.268836409340478e-5
allele num: 120936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.461-18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.698-18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*441-18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.611-18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1901-18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.842-18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1230-18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.548-18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*531-18G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.445-18G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-134131154-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131154
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131154
    reference: chr 11
allele count: 10
allele frequency: 8.26255081468751e-5
allele num: 121028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.461-15G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*531-15G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.445-15G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.548-15G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*441-15G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.698-15G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1230-15G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.611-15G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1901-15G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.842-15G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27425
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-134131161-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131161
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131161
    reference: chr 11
allele count: 219
allele frequency: 1.806751806751807e-3
allele num: 121212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.461-8C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.698-8C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1901-8C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.445-8C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*531-8C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*441-8C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.548-8C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.842-8C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1230-8C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.611-8C>G
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 8.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6226
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17628
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 6.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 27421
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
hgvs: c.842-8C>G
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-134131172-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131172
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131172
    reference: chr 11
allele count: 6
allele frequency: 4.945516888940176e-5
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.464C>T
  hgvsp: ENSP00000363884.4:p.Ser155Phe
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.551C>T
  hgvsp: ENSP00000438302.1:p.Ser184Phe
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.845C>T
  hgvsp: ENSP00000281182.4:p.Ser282Phe
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1233C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.448C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.701C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.614C>T
  hgvsp: ENSP00000443763.1:p.Ser205Phe
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1904C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*534C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*444C>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser282Phe
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

11-134131173-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131173
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131173
    reference: chr 11
allele count: 7
allele frequency: 5.76948437293947e-5
allele num: 121328
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.846C>G
  hgvsp: ENST00000281182.4:c.846C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.465C>G
  hgvsp: ENST00000374752.4:c.465C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.552C>G
  hgvsp: ENST00000543332.1:c.552C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1234C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*445C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.615C>G
  hgvsp: ENST00000537423.1:c.615C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.702C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.449C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*535C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1905C>G
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser282Ser
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

11-134131173-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131173
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131173
    reference: chr 11
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1905C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*535C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*445C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1234C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.552C>T
  hgvsp: ENST00000543332.1:c.552C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.465C>T
  hgvsp: ENST00000374752.4:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.846C>T
  hgvsp: ENST00000281182.4:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.615C>T
  hgvsp: ENST00000537423.1:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.449C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.702C>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1408
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7350
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser282Ser
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-134131180-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131180
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131180
    reference: chr 11
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.472C>G
  hgvsp: ENSP00000363884.4:p.Leu158Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.709C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.853C>G
  hgvsp: ENSP00000281182.4:p.Leu285Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.456C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.622C>G
  hgvsp: ENSP00000443763.1:p.Leu208Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1912C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.559C>G
  hgvsp: ENSP00000438302.1:p.Leu187Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*542C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1241C>G
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*452C>G
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu285Val
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

11-134131182-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131182
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131182
    reference: chr 11
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1243G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.855G>A
  hgvsp: ENST00000281182.4:c.855G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.711G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.561G>A
  hgvsp: ENST00000543332.1:c.561G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.458G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1914G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.474G>A
  hgvsp: ENST00000374752.4:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.624G>A
  hgvsp: ENST00000537423.1:c.624G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*454G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*544G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu285Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

11-134131187-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131187
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131187
    reference: chr 11
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1248C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1919C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.716C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.860C>T
  hgvsp: ENSP00000281182.4:p.Ala287Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*459C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.566C>T
  hgvsp: ENSP00000438302.1:p.Ala189Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.463C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.629C>T
  hgvsp: ENSP00000443763.1:p.Ala210Val
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*549C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.479C>T
  hgvsp: ENSP00000363884.4:p.Ala160Val
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2462
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala287Val
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: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

11-134131189-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131189
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131189
    reference: chr 11
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1921G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.568G>A
  hgvsp: ENSP00000438302.1:p.Ala190Thr
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.718G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.481G>A
  hgvsp: ENSP00000363884.4:p.Ala161Thr
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*461G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.465G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.631G>A
  hgvsp: ENSP00000443763.1:p.Ala211Thr
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.862G>A
  hgvsp: ENSP00000281182.4:p.Ala288Thr
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1250G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*551G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala288Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-134131194-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131194
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131194
    reference: chr 11
allele count: 3
allele frequency: 2.471495419495156e-5
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.636C>T
  hgvsp: ENST00000537423.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.867C>T
  hgvsp: ENST00000281182.4:c.867C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1255C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.573C>T
  hgvsp: ENST00000543332.1:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.470C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1926C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*556C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*466C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.723C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.486C>T
  hgvsp: ENST00000374752.4:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His289His
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

11-134131195-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131195
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131195
    reference: chr 11
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.574G>A
  hgvsp: ENSP00000438302.1:p.Ala192Thr
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*557G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.637G>A
  hgvsp: ENSP00000443763.1:p.Ala213Thr
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.724G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1256G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.487G>A
  hgvsp: ENSP00000363884.4:p.Ala163Thr
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1927G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*467G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.868G>A
  hgvsp: ENSP00000281182.4:p.Ala290Thr
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.471G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala290Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

11-134131195-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131195
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131194
    reference: chr 11
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.870delC
  hgvsp: ENSP00000281182.4:p.Ser291LeufsTer41
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1258delC
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.473delC
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.726delC
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.639delC
  hgvsp: ENSP00000443763.1:p.Ser214LeufsTer41
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.489delC
  hgvsp: ENSP00000363884.4:p.Ser164LeufsTer41
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*469delC
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.576delC
  hgvsp: ENSP00000438302.1:p.Ser193LeufsTer29
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1929delC
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*559delC
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser291LeufsTer41
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: GC
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

11-134131201-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131201
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131201
    reference: chr 11
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*473G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.493G>A
  hgvsp: ENSP00000363884.4:p.Val165Ile
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*563G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1933G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.643G>A
  hgvsp: ENSP00000443763.1:p.Val215Ile
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.874G>A
  hgvsp: ENSP00000281182.4:p.Val292Ile
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.580G>A
  hgvsp: ENSP00000438302.1:p.Val194Ile
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1262G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.730G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.477G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val292Ile
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

11-134131209-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131209
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131209
    reference: chr 11
allele count: 4
allele frequency: 3.295272930980509e-5
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*571C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.588C>T
  hgvsp: ENST00000543332.1:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.738C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.651C>T
  hgvsp: ENST00000537423.1:c.651C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.882C>T
  hgvsp: ENST00000281182.4:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1270C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*481C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.485C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.501C>T
  hgvsp: ENST00000374752.4:c.501C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1941C>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7285
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu294Leu
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

11-134131213-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131213
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131213
    reference: chr 11
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.742C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*485C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.505C>T
  hgvsp: ENSP00000363884.4:p.Arg169Ter
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.655C>T
  hgvsp: ENSP00000443763.1:p.Arg219Ter
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.592C>T
  hgvsp: ENSP00000438302.1:p.Arg198Ter
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.886C>T
  hgvsp: ENSP00000281182.4:p.Arg296Ter
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.489C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*575C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1945C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1274C>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg296Ter
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

11-134131214-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131214
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131214
    reference: chr 11
allele count: 18
allele frequency: 1.482799525504152e-4
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*486G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.593G>A
  hgvsp: ENSP00000438302.1:p.Arg198Gln
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.656G>A
  hgvsp: ENSP00000443763.1:p.Arg219Gln
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1275G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.490G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.887G>A
  hgvsp: ENSP00000281182.4:p.Arg296Gln
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.506G>A
  hgvsp: ENSP00000363884.4:p.Arg169Gln
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1946G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*576G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.743G>A
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg296Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

11-134131222-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131222
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131222
    reference: chr 11
allele count: 3
allele frequency: 2.471413978317461e-5
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.514C>T
  hgvsp: ENSP00000363884.4:p.Leu172Phe
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.664C>T
  hgvsp: ENSP00000443763.1:p.Leu222Phe
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.498C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1283C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1954C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.601C>T
  hgvsp: ENSP00000438302.1:p.Leu201Phe
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*584C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*494C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.895C>T
  hgvsp: ENSP00000281182.4:p.Leu299Phe
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.751C>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7380
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu299Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

11-134131231-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131231
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131231
    reference: chr 11
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*503C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1292C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.523C>T
  hgvsp: ENSP00000363884.4:p.Arg175Trp
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.507C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.610C>T
  hgvsp: ENSP00000438302.1:p.Arg204Trp
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.673C>T
  hgvsp: ENSP00000443763.1:p.Arg225Trp
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*593C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.760C>T
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.904C>T
  hgvsp: ENSP00000281182.4:p.Arg302Trp
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1963C>T
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17858
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg302Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

11-134131232-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131232
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131232
    reference: chr 11
allele count: 5
allele frequency: 4.118955432902216e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.905G>A
  hgvsp: ENSP00000281182.4:p.Arg302Gln
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.674G>A
  hgvsp: ENSP00000443763.1:p.Arg225Gln
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.761G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.611G>A
  hgvsp: ENSP00000438302.1:p.Arg204Gln
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.508G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*594G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1293G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*504G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1964G>A
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.524G>A
  hgvsp: ENSP00000363884.4:p.Arg175Gln
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg302Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-134131242-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131242
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131242
    reference: chr 11
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*604T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000533387
  gene symbol: ACAD8
  hgvsc: ENST00000533387.1:n.1974T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000524547
  gene symbol: ACAD8
  hgvsc: ENST00000524547.1:n.518T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000281182
  ensembl transcript: ENST00000281182
  gene symbol: ACAD8
  hgvsc: ENST00000281182.4:c.915T>C
  hgvsp: ENST00000281182.4:c.915T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000363884
  ensembl transcript: ENST00000374752
  gene symbol: ACAD8
  hgvsc: ENST00000374752.4:c.534T>C
  hgvsp: ENST00000374752.4:c.534T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000531338
  gene symbol: ACAD8
  hgvsc: ENST00000531338.1:n.771T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000438302
  ensembl transcript: ENST00000543332
  gene symbol: ACAD8
  hgvsc: ENST00000543332.1:c.621T>C
  hgvsp: ENST00000543332.1:c.621T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431310
  ensembl transcript: ENST00000524426
  gene symbol: ACAD8
  hgvsc: ENST00000524426.1:c.*514T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151498
  ensembl transcript: ENST00000527665
  gene symbol: ACAD8
  hgvsc: ENST00000527665.1:n.1303T>C
  variant of: http://identifiers.org/hgnc/87
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000443763
  ensembl transcript: ENST00000537423
  gene symbol: ACAD8
  hgvsc: ENST00000537423.1:c.684T>C
  hgvsp: ENST00000537423.1:c.684T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2471
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe305Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-134131244-GAGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134131244
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 134131241
    reference: chr 11
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151498
  ensembl protein: ENSP00000431532
  ensembl transcript: ENST00000526026
  gene symbol: ACAD8
  hgvsc: ENST00000526026.1:c.*607_*609delAGA
  variant of: http://identifiers.org/hgnc/87
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
hgvs: p.Glu307del
num of homozygotes: 0
reference allele: GAGA

GenotypeDepth
all individuals: 11909
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9232
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19974
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4298
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6966
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 765
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3770
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2433
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1643
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12646
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8878
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9442
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.711496746203905e-4
allele num: 7376
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4784
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.28355054596689e-5
allele num: 56780
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

DP
type: SiteQuality
SIO_000300: 1.421014e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.516e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

QD
type: SiteQuality
SIO_000300: 1.258e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.868e0

MQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

GenotypeQuality
all individuals: 316
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21302
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4074
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3617
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12420
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1435
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2202
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6969
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 516
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8926
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13762
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.726003490401397e-5
allele num: 57300
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.162e0

DP
type: SiteQuality
SIO_000300: 1.433987e6

VQSLOD
type: SiteQuality
SIO_000300: -1.071e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

QD
type: SiteQuality
SIO_000300: 1.999e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

GenotypeQuality
all individuals: 820
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12007
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2680
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3773
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22788
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3456
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2027
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6963
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 202
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 527
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13848
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8978
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.728668233992532e-5
allele num: 57848
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9564
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.231e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

FS
type: SiteQuality
SIO_000300: 1.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.92e-1

DP
type: SiteQuality
SIO_000300: 1.452632e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.96e-1

QD
type: SiteQuality
SIO_000300: 6.33e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1997
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23429
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3716
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12004
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2730
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3431
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 827
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6963
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.72188167229148e-5
allele num: 58076
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4928
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13878
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9012
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 1.067e1

FS
type: SiteQuality
SIO_000300: 7.768e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

VQSLOD
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 1.455074e6

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.283e0

GenotypeQuality
all individuals: 1413
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6962
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 296
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11994
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2359
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3986
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3562
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21496
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2634
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13972
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9052
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.706542885422711e-5
allele num: 58598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4954
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.878e-1

QD
type: SiteQuality
SIO_000300: 1.641e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 2.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.643e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 1.459337e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.89e0

GenotypeQuality
all individuals: 319
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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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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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 527
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13968
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.705844222305619e-5
allele num: 58622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4954
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.95e-1

FS
type: SiteQuality
SIO_000300: 6.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.588e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.54e-1

QD
type: SiteQuality
SIO_000300: 8.6e0

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

DP
type: SiteQuality
SIO_000300: 1.459532e6

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9050
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9554
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4954
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.411688444611238e-5
allele num: 58622
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13968
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7642
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

InbreedingCoeff
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SIO_000300: 2.4e-3

FS
type: SiteQuality
SIO_000300: 6.71e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.588e-1

DP
type: SiteQuality
SIO_000300: 1.459532e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.95e-1

QD
type: SiteQuality
SIO_000300: 8.6e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2620
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variant carriers: 0

GenotypeQuality
all individuals: 3617
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.411339291805963e-5
allele num: 58628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4966
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.162297665090961e-5
allele num: 13962
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.311991603253739e-4
allele num: 7622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.146e1

VQSLOD
type: SiteQuality
SIO_000300: 3.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.44e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.01e-1

DP
type: SiteQuality
SIO_000300: 1.460555e6

GenotypeQuality
all individuals: 1016
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
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GenotypeQuality
all individuals: 4213
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6973
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variant carriers: 8

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11997
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variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4960
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9058
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 1.048218029350105e-3
allele num: 9540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.45344e6

MQRankSum
type: SiteQuality
SIO_000300: 1.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

FS
type: SiteQuality
SIO_000300: 8.148999999999999e0

QD
type: SiteQuality
SIO_000300: 1.205e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 11986
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13986
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7656
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.701374710766299e-5
allele num: 58776
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9060
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4948
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.449762e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.475e0

ClippingRankSum
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QD
type: SiteQuality
SIO_000300: 3.042e1

MQRankSum
type: SiteQuality
SIO_000300: -1.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.556e0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.509769215058888e-5
allele num: 58756
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9040
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.02020202020202e-4
allele num: 4950
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9498
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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DP
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MQRankSum
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QD
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FS
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
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SIO_000300: -2.12e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59134
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.301744337412132e-4
allele num: 7682
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5000
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14034
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
allele num: 9514
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
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BaseQRankSum
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DP
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QD
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FS
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.58732212160414e-4
allele num: 7730
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14098
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5024
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.324e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.02e0

FS
type: SiteQuality
SIO_000300: 1.1662e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.272e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.73e-1

DP
type: SiteQuality
SIO_000300: 1.454761e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4450
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9166
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14096
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5022
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 9.107468123861566e-4
allele num: 7686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59388
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

DP
type: SiteQuality
SIO_000300: 1.455225e6

VQSLOD
type: SiteQuality
SIO_000300: 3.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.799e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.25e-1

QD
type: SiteQuality
SIO_000300: 1.257e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 6

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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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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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1316
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14072
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5020
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.57030223390276e-4
allele num: 9132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7700
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.02e-1

DP
type: SiteQuality
SIO_000300: 1.457396e6

VQSLOD
type: SiteQuality
SIO_000300: 2.1e0

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.53e-1

QD
type: SiteQuality
SIO_000300: 1.318e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.093e0

GenotypeQuality
all individuals: 1059
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2922
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1277
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
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variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18674
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variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6974
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7738
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5036
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9436
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.35750738651625e-5
allele num: 59568
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

DP
type: SiteQuality
SIO_000300: 1.459599e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

QD
type: SiteQuality
SIO_000300: 1.027e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.837999999999999e0

GenotypeQuality
all individuals: 2075
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 5.75e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 286
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7744
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5082
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.079144839303412e-5
allele num: 14126
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.988e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.217e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

FS
type: SiteQuality
SIO_000300: 2.923e0

DP
type: SiteQuality
SIO_000300: 1.462499e6

QD
type: SiteQuality
SIO_000300: 1.285e1

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: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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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: 17562
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5068
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9394
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.061149555147578e-5
allele num: 14162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7708
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.672128954584977e-5
allele num: 59804
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.051e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

DP
type: SiteQuality
SIO_000300: 1.47223e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.51e-1

QD
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SIO_000300: 8.199999999999999e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 6989
bin: 9.75e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.664004259850905e-5
allele num: 60096
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.327131112072696e-4
allele num: 9244
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14206
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7724
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5102
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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QD
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ClippingRankSum
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SIO_000300: -1.97e-1

InbreedingCoeff
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SIO_000300: -2.9e-3

DP
type: SiteQuality
SIO_000300: 1.478822e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1211
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 340
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variant carriers: 0

GenotypeQuality
all individuals: 10045
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7784
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.648913366091746e-5
allele num: 60646
num of homozygotes: 0

African
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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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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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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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BaseQRankSum
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SIO_000300: -4.034e0

QD
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GenotypeQuality
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GenotypeQuality
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variant carriers: 212

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61010
num of homozygotes: 0

African
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allele count: 212
allele frequency: 2.261574567953915e-2
allele num: 9374
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South Asian
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allele frequency: 0.0e0
allele num: 14392
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 5262
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

Latino
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allele count: 12
allele frequency: 1.23787910047452e-3
allele num: 9694
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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DP
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SIO_000300: 1.521386e6

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 5
allele frequency: 8.168333006600014e-5
allele num: 61212
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7860
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5294
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.525121e6

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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ReadPosRankSum
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SIO_000300: 2.9e-1

MQRankSum
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SIO_000300: 4.5e-1

FS
type: SiteQuality
SIO_000300: 3.324e0

InbreedingCoeff
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SIO_000300: 2.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.55e-1

QD
type: SiteQuality
SIO_000300: 1.024e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9412
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7860
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14424
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5294
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.633666601320003e-5
allele num: 61212
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.324e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 6.3e-1

BaseQRankSum
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SIO_000300: 7.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

QD
type: SiteQuality
SIO_000300: 1.024e1

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-1

DP
type: SiteQuality
SIO_000300: 1.525121e6

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5408
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61748
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9492
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.859651529702291e-5
allele num: 14578
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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FS
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SIO_000300: 0.0e0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7962
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.837773334193382e-5
allele num: 62012
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5472
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African
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QD
type: SiteQuality
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FS
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQ
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VQSLOD
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10048
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5486
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South Asian
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allele frequency: 6.78334011667345e-5
allele num: 14742
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: -1.7e-3

ClippingRankSum
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MQ
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BaseQRankSum
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FS
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MQRankSum
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VQSLOD
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DP
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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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variant carriers: 2

GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8012
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.354096140825999e-4
allele num: 14770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62410
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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BaseQRankSum
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DP
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MQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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ClippingRankSum
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VQSLOD
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SIO_000300: -2.274e0

QD
type: SiteQuality
SIO_000300: 1.174e1

GenotypeQuality
all individuals: 4959
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28562
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1665
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1697
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6235
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2049
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7037
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10424
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15076
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63196
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.030715316429602e-4
allele num: 9702
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.777e0

QD
type: SiteQuality
SIO_000300: 2.099e1

FS
type: SiteQuality
SIO_000300: 7.684e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQRankSum
type: SiteQuality
SIO_000300: 6.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 1.628656e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.722e0

GenotypeDepth
all individuals: 713
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 560
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1363
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4980
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6157
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1863
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29149
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63230
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.63129973474801e-5
allele num: 15080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5758
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10434
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.077e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.631661e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

QD
type: SiteQuality
SIO_000300: 1.131e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

GenotypeQuality
all individuals: 456
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 82
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7044
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1664
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
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variant carriers: 0

GenotypeQuality
all individuals: 5306
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variant carriers: 0

GenotypeQuality
all individuals: 1600
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variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31079
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1776
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8240
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5874
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.878992859827133e-4
allele num: 10644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.27549419516787e-5
allele num: 63740
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

FS
type: SiteQuality
SIO_000300: 5.565e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

DP
type: SiteQuality
SIO_000300: 1.660608e6

QD
type: SiteQuality
SIO_000300: 1.401e1

MQRankSum
type: SiteQuality
SIO_000300: -3.85e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
all individuals: 5146
bin: 6.75e1
variant carriers: 9

GenotypeQuality
all individuals: 712
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1706
bin: 7.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1603
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 37
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variant carriers: 1

GenotypeQuality
all individuals: 467
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1626
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8277
bin: 9.75e1
variant carriers: 1585

GenotypeQuality
all individuals: 749
bin: 4.75e1
variant carriers: 7

GenotypeQuality
all individuals: 948
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 29601
bin: 6.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1048
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1716
bin: 7.25e1
variant carriers: 9

GenotypeQuality
all individuals: 5101
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 99
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 384
bin: 9.25e1
variant carriers: 6

GenotypeQuality
all individuals: 98
bin: 1.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5882
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.667481662591687e-3
allele num: 818
num of homozygotes: 0

Latino
type: Population
allele count: 77
allele frequency: 7.223264540337711e-3
allele num: 10660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 2.978149785259726e-4
allele num: 63798
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8258
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.620545073375262e-4
allele num: 15264
num of homozygotes: 0

African
type: Population
allele count: 1681
allele frequency: 1.693873438129786e-1
allele num: 9924
num of homozygotes: 127

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.692244e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.212e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.57e0

QD
type: SiteQuality
SIO_000300: 1.594e1

VQSLOD
type: SiteQuality
SIO_000300: 6.32e0

GenotypeQuality
all individuals: 5328
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1068
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5029
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variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 514
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variant carriers: 0

GenotypeQuality
all individuals: 441
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variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 30094
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variant carriers: 0

GenotypeQuality
all individuals: 1596
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 988
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variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1777
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7089
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 415
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.723111626304082e-4
allele num: 63838
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.20918984280532e-4
allele num: 8270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9926
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

QD
type: SiteQuality
SIO_000300: 1.419e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.03e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

DP
type: SiteQuality
SIO_000300: 1.675557e6

FS
type: SiteQuality
SIO_000300: 5.21e-1

GenotypeQuality
all individuals: 98
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5407
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
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GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
all individuals: 772
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variant carriers: 0

GenotypeQuality
all individuals: 30619
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1053
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 580
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variant carriers: 0

GenotypeQuality
all individuals: 1585
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7084
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 441
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GenotypeQuality
all individuals: 888
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variant carriers: 0

GenotypeQuality
all individuals: 1815
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15320
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5922
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.563966218329684e-5
allele num: 63940
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.79e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.341e-1

QD
type: SiteQuality
SIO_000300: 1.249e1

FS
type: SiteQuality
SIO_000300: 1.368e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 1.680738e6

MQ
type: SiteQuality
SIO_000300: 5.933e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.588e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e0

GenotypeQuality
all individuals: 85
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4469
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 1558
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variant carriers: 0

GenotypeQuality
all individuals: 86
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GenotypeQuality
all individuals: 1128
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GenotypeQuality
all individuals: 417
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variant carriers: 0

GenotypeQuality
all individuals: 5331
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variant carriers: 0

GenotypeQuality
all individuals: 134
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variant carriers: 0

GenotypeQuality
all individuals: 438
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variant carriers: 0

GenotypeQuality
all individuals: 1474
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variant carriers: 0

GenotypeQuality
all individuals: 7084
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1691
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variant carriers: 0

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

GenotypeQuality
all individuals: 869
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1824
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9966
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6002
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.557875058420315e-5
allele num: 64190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8336
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.24898261191269e-5
allele num: 10812
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e0

VQSLOD
type: SiteQuality
SIO_000300: -6.98e-1

QD
type: SiteQuality
SIO_000300: 7.74e0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.74e-1

FS
type: SiteQuality
SIO_000300: 1.145e0

DP
type: SiteQuality
SIO_000300: 1.693791e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 7086
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
all individuals: 557
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GenotypeQuality
all individuals: 21
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1232
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variant carriers: 0

GenotypeQuality
all individuals: 170
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variant carriers: 0

GenotypeQuality
all individuals: 5387
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variant carriers: 0

GenotypeQuality
all individuals: 1679
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variant carriers: 0

GenotypeQuality
all individuals: 29733
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variant carriers: 0

GenotypeQuality
all individuals: 445
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GenotypeQuality
all individuals: 1331
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GenotypeQuality
all individuals: 4277
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variant carriers: 0

GenotypeQuality
all individuals: 1048
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variant carriers: 0

GenotypeQuality
all individuals: 1845
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1277
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1801
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.556468683850081e-5
allele num: 64248
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6038
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8354
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.70119e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.95e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.658e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 6.67e0

MQRankSum
type: SiteQuality
SIO_000300: -8.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.57e-1

FS
type: SiteQuality
SIO_000300: 8.471e0

VQSLOD
type: SiteQuality
SIO_000300: -2.021e0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1520
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31191
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1845
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3936
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5537
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1899
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7089
bin: 9.75e1
variant carriers: 4

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10022
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10926
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.201358097423335e-5
allele num: 64502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6102
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

FS
type: SiteQuality
SIO_000300: 6.643e0

MQ
type: SiteQuality
SIO_000300: 5.833e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

DP
type: SiteQuality
SIO_000300: 1.715464e6

GenotypeQuality
all individuals: 1059
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1220
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 287
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1868
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 230
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30575
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 965
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3475
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1817
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7042
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1065
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 440
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 835
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.80635838150289e-4
allele num: 5536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.557792787052377e-5
allele num: 62776
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15658
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8326
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.071680132587529e-4
allele num: 9654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10894
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.307e0

FS
type: SiteQuality
SIO_000300: 1.40099e2

VQSLOD
type: SiteQuality
SIO_000300: -9.359e1

MQ
type: SiteQuality
SIO_000300: 5.82e1

QD
type: SiteQuality
SIO_000300: 5.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.37e0

DP
type: SiteQuality
SIO_000300: 1.724003e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQRankSum
type: SiteQuality
SIO_000300: -6.16e-1

GenotypeQuality
all individuals: 980
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 7126
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1921
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1894
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 29003
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1309
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1339
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 473
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5410
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1533
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558166349839509e-5
allele num: 64178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9902
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.575402635431918e-4
allele num: 10928
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15646
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.934e0

QD
type: SiteQuality
SIO_000300: 9.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.16e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 1.718209e6

GenotypeQuality
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2828
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6374
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7206
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2187
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1293
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32286
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.352941176470588e-4
allele num: 8500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6264
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11108
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.992428770671449e-4
allele num: 10038
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.32351081320349e-5
allele num: 15814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64930
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.39e-1

QD
type: SiteQuality
SIO_000300: 1.184e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 1.743934e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

GenotypeQuality
all individuals: 880
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2828
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7206
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 670
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32286
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 6374
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 514
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variant carriers: 0

GenotypeQuality
all individuals: 2187
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540120129370091e-5
allele num: 64930
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6264
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15814
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.39e-1

DP
type: SiteQuality
SIO_000300: 1.743934e6

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

QD
type: SiteQuality
SIO_000300: 1.184e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

GenotypeQuality
all individuals: 47
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2388
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 438
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variant carriers: 0

GenotypeQuality
all individuals: 2235
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variant carriers: 0

GenotypeQuality
all individuals: 6478
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variant carriers: 0

GenotypeQuality
all individuals: 7365
bin: 9.75e1
variant carriers: 187

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 826
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 545
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variant carriers: 0

GenotypeQuality
all individuals: 513
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variant carriers: 0

GenotypeQuality
all individuals: 976
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variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33093
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.282985674792661e-5
allele num: 15916
num of homozygotes: 0

Latino
type: Population
allele count: 20
allele frequency: 1.788908765652952e-3
allele num: 11180
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.464203233256351e-3
allele num: 866
num of homozygotes: 0

African
type: Population
allele count: 130
allele frequency: 1.290706910246227e-2
allele num: 10072
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 33
allele frequency: 5.067567567567568e-4
allele num: 65120
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.763971e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

FS
type: SiteQuality
SIO_000300: 5.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.36e-1

QD
type: SiteQuality
SIO_000300: 1.48e1

GenotypeQuality
all individuals: 493
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2193
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
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variant carriers: 0

GenotypeQuality
all individuals: 435
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 6576
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variant carriers: 0

GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 298
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GenotypeQuality
all individuals: 532
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GenotypeQuality
all individuals: 393
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2253
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7222
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 1
allele frequency: 8.914244963451596e-5
allele num: 11218
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.908838684106223e-5
allele num: 10092
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15954
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6356
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65218
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.45e-1

MQ
type: SiteQuality
SIO_000300: 5.801e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.86e-1

QD
type: SiteQuality
SIO_000300: 1.422e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.866e-1

DP
type: SiteQuality
SIO_000300: 1.768368e6

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

GenotypeQuality
all individuals: 655
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 34339
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
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variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2298
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 771
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variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1338
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6726
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.877840909090909e-5
allele num: 11264
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.52849107361213e-5
allele num: 65424
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16048
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10112
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: 8.59e-1

InbreedingCoeff
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SIO_000300: 1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.11e-1

FS
type: SiteQuality
SIO_000300: 1.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.07e-1

DP
type: SiteQuality
SIO_000300: 1.775812e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.238e0

QD
type: SiteQuality
SIO_000300: 1.381e1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65928
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.72e-1

QD
type: SiteQuality
SIO_000300: 1.164e1

MQ
type: SiteQuality
SIO_000300: 5.932e1

FS
type: SiteQuality
SIO_000300: 7.191e0

VQSLOD
type: SiteQuality
SIO_000300: -2.169e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 1.802112e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.985e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.347e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513867021920794e-5
allele num: 66056
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16326
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.838e1

QD
type: SiteQuality
SIO_000300: 1.671e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.810424e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.43e0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.516303856923494e-5
allele num: 66426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.939864209505335e-4
allele num: 10310
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 1.225e0

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.88e-1

DP
type: SiteQuality
SIO_000300: 1.829798e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.995e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.241e1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.69414014953921e-5
allele num: 11502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.009238361770636e-5
allele num: 66462
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.831787e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.331e1

MQ
type: SiteQuality
SIO_000300: 5.941e1

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.57e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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allele frequency: 0.0e0
allele num: 900
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 3
allele frequency: 1.82370820668693e-4
allele num: 16450
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.052504961809106e-4
allele num: 66508
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East Asian
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
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Latino
type: Population
allele count: 0
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allele num: 11512
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.28e-1

QD
type: SiteQuality
SIO_000300: 1.497e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.13e-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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Latino
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allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

African
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East Asian
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allele count: 8
allele frequency: 9.250693802035153e-4
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50271992306074e-5
allele num: 66546
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European (Finnish)
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allele count: 1
allele frequency: 1.518372304889159e-4
allele num: 6586
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Other
type: Population
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South Asian
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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VQSLOD
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MQRankSum
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MQ
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FS
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
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African
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Latino
type: Population
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allele frequency: 8.664009703690868e-5
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Other
type: Population
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East Asian
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European (Non-Finnish)
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allele count: 205
allele frequency: 3.075861241147521e-3
allele num: 66648
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European (Finnish)
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allele count: 12
allele frequency: 1.818181818181818e-3
allele num: 6600
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DP
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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Latino
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European (Non-Finnish)
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South Asian
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FS
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InbreedingCoeff
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DP
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BaseQRankSum
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QD
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ClippingRankSum
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VQSLOD
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MQRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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Other
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DP
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QD
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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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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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Other
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European (Finnish)
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South Asian
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European (Non-Finnish)
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VQSLOD
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DP
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QD
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FS
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MQRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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FS
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DP
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MQRankSum
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ClippingRankSum
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QD
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MQ
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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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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InbreedingCoeff
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ClippingRankSum
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QD
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MQ
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FS
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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DP
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ReadPosRankSum
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FS
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VQSLOD
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MQ
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QD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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European (Non-Finnish)
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African
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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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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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MQ
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FS
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DP
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ClippingRankSum
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InbreedingCoeff
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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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Latino
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European (Non-Finnish)
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ReadPosRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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QD
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MQRankSum
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MQ
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ClippingRankSum
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11576
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

African
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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: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

Other
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DP
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BaseQRankSum
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FS
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SIO_000300: 1.148e0

InbreedingCoeff
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SIO_000300: 1.0e-4

VQSLOD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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SIO_000300: -8.699999999999999e-2

MQ
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SIO_000300: 5.979e1

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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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

African
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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
allele num: 6614
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

East Asian
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allele count: 4
allele frequency: 4.622140050843541e-4
allele num: 8654
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66720
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European (Finnish)
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allele count: 0
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: -3.64e-1

BaseQRankSum
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MQ
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SIO_000300: 5.961e1

MQRankSum
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InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

ReadPosRankSum
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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ClippingRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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QD
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FS
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VQSLOD
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66724
num of homozygotes: 0

European (Finnish)
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Latino
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African
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South Asian
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Other
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East Asian
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MQRankSum
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VQSLOD
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ReadPosRankSum
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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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FS
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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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European (Finnish)
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num of homozygotes: 0

Latino
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Other
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European (Non-Finnish)
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allele num: 66724
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African
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East Asian
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South Asian
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FS
type: SiteQuality
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MQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66726
num of homozygotes: 0

European (Finnish)
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Other
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South Asian
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Latino
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African
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East Asian
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.929e1

FS
type: SiteQuality
SIO_000300: 3.126e0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 1.845624e6

QD
type: SiteQuality
SIO_000300: 1.203e1

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 564
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7369
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2469
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2478
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7286
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 38525
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 5
allele frequency: 4.319281271596407e-4
allele num: 11576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.845946e6

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.32e-1

QD
type: SiteQuality
SIO_000300: 1.117e1

FS
type: SiteQuality
SIO_000300: 2.494e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

MQRankSum
type: SiteQuality
SIO_000300: 3.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.88e-1

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

GenotypeQuality
all individuals: 2477
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 564
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7364
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7282
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 38513
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.347e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-1

DP
type: SiteQuality
SIO_000300: 1.845669e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.158e0