12-112123637-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112123637
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112123637
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 39472
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089234
  ensembl protein: ENSP00000403524
  ensembl transcript: ENST00000419234
  gene symbol: BRAP
  hgvsc: ENST00000419234.4:c.-41G>A
  variant of: http://identifiers.org/hgnc/1099
canonical: true
consequence: 5' UTR
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19763
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15743
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2318
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2652
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21498
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18889
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1997
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3595
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1364
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1028
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8736
  num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

12-112130463-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130463
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130463
    reference: chr 12
allele count: 2
allele frequency: 1.743952843515111e-5
allele num: 114682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.173-38T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.173-38T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6420T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.160-38T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1025-38T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-13-38T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-13-38T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.185-38T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-13-38T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-13-38T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-13-38T>C
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12008
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

12-112130463-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130463
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130463
    reference: chr 12
allele count: 427
allele frequency: 3.723339320904763e-3
allele num: 114682
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1025-38T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-13-38T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.173-38T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-13-38T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-13-38T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-13-38T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.185-38T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.173-38T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-13-38T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6420T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.160-38T>G
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 6.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 5.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 12008
  bin: 3.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 15345
  bin: 2.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 4.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 4.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7229
  bin: 3.75e1
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

12-112130466-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130466
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130466
    reference: chr 12
allele count: 2
allele frequency: 1.74377038031632e-5
allele num: 114694
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.173-35A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.173-35A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6423A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-13-35A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-13-35A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.185-35A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-13-35A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-13-35A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-13-35A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.160-35A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1025-35A>G
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7229
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15130
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

12-112130467-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130467
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130467
    reference: chr 12
allele count: 1
allele frequency: 8.717027842186928e-6
allele num: 114718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-13-34G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-13-34G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1025-34G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.160-34G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6424G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.185-34G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-13-34G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-13-34G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.173-34G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-13-34G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.173-34G>A
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3028
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

12-112130473-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130473
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130473
    reference: chr 12
allele count: 1
allele frequency: 8.707464038173523e-6
allele num: 114844
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.160-28T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1025-28T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.173-28T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-13-28T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-13-28T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-13-28T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.173-28T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-13-28T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-13-28T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6430T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.185-28T>G
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

12-112130476-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130476
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130476
    reference: chr 12
allele count: 1
allele frequency: 8.694291328313829e-6
allele num: 115018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-13-25C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6433C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-13-25C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1025-25C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.185-25C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-13-25C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.173-25C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.160-25C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.173-25C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-13-25C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-13-25C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12114
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

12-112130480-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130480
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130480
    reference: chr 12
allele count: 1
allele frequency: 8.664309974353643e-6
allele num: 115416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-13-21C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-13-21C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-13-21C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1025-21C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.173-21C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.173-21C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-13-21C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.185-21C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.160-21C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-13-21C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6437C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4858
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2619
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

12-112130482-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130482
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130482
    reference: chr 12
allele count: 2
allele frequency: 1.729984084146426e-5
allele num: 115608
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1025-19G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.173-19G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.185-19G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-13-19G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-13-19G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-13-19G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.160-19G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6439G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-13-19G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-13-19G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.173-19G>A
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15671
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

12-112130486-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130486
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130486
    reference: chr 12
allele count: 1
allele frequency: 8.62083829031535e-6
allele num: 115998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-13-15C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.185-15C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.173-15C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6443C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.173-15C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1025-15C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.160-15C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-13-15C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-13-15C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-13-15C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-13-15C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

12-112130489-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130489
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130489
    reference: chr 12
allele count: 1
allele frequency: 8.605851979345956e-6
allele num: 116200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.185-12C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-13-12C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.173-12C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-13-12C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.173-12C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.160-12C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1025-12C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-13-12C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-13-12C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6446C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-13-12C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

12-112130490-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130490
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130490
    reference: chr 12
allele count: 627
allele frequency: 5.38891276321444e-3
allele num: 116350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1025-11T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-13-11T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-13-11T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.173-11T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-13-11T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-13-11T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6447T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.185-11T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-13-11T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.173-11T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.160-11T>C
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 6.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 5.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 12087
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 5491
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 4.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 15718
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 155
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 5.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 4811
  bin: 4.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 50
genotype quality: GenotypeQuality
  all individuals: 18621
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 22
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

12-112130495-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130495
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130495
    reference: chr 12
allele count: 1
allele frequency: 8.547446877617655e-6
allele num: 116994
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-13-6A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.173-6A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.185-6A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.173-6A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-13-6A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6452A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-13-6A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1025-6A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-13-6A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.160-6A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-13-6A>G
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.-13-6A>G
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

12-112130496-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130496
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130496
    reference: chr 12
allele count: 12
allele frequency: 1.025500786217269e-4
allele num: 117016
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-13-5C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-13-5C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-13-5C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.173-5C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.173-5C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.160-5C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.185-5C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1025-5C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-13-5C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6453C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-13-5C>G
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5904
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12119
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: c.-13-5C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

12-112130501-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130501
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130501
    reference: chr 12
allele count: 1
allele frequency: 8.498920637079091e-6
allele num: 117662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6458C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-13C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1025C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-13C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.185C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-13C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.173C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.173C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-13C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-13C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.160C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.-13C>T
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-112130510-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130510
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130510
    reference: chr 12
allele count: 1
allele frequency: 8.404915194405689e-6
allele num: 118978
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.-4C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.-4C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.182C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.194C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1016C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.182C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.169C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6467C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7146
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

12-112130514-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130514
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130514
    reference: chr 12
allele count: 1
allele frequency: 8.370302167908262e-6
allele num: 119470
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1012A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.1A>G
  hgvsp: ENSP00000446998.1:p.Met1?
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.1A>G
  hgvsp: ENSP00000446959.1:p.Met1?
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.1A>G
  hgvsp: ENSP00000389813.2:p.Met1?
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.186A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.1A>G
  hgvsp: ENSP00000421527.1:p.Met1?
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6471A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.186A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.1A>G
  hgvsp: ENSP00000325137.4:p.Met1?
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.198A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.173A>G
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: start lost
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum

12-112130520-GTCAGGAGCTGTTTCCAGTCCC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130520
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130499
    reference: chr 12
allele count: 1
allele frequency: 8.342092530490349e-6
allele num: 119874
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsp: ENSP00000446959.1:p.Val3_Pro10delinsAla
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsp: ENSP00000325137.4:p.Val3_Pro10delinsAla
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsp: ENSP00000421527.1:p.Val3_Pro10delinsAla
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsp: ENSP00000389813.2:p.Val3_Pro10delinsAla
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsp: ENSP00000446998.1:p.Val3_Pro10delinsAla
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3417
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val3_Pro10delinsAla
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: GTCAGGAGCTGTTTCCAGTCCC
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

12-112130525-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130525
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130525
    reference: chr 12
allele count: 1
allele frequency: 8.30813199960121e-6
allele num: 120364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.12G>T
  hgvsp: ENSP00000421527.1:p.Arg4Ser
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.12G>T
  hgvsp: ENSP00000325137.4:p.Arg4Ser
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.184G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6482G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.197G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-1001G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.197G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.12G>T
  hgvsp: ENSP00000446998.1:p.Arg4Ser
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.12G>T
  hgvsp: ENSP00000446959.1:p.Arg4Ser
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.209G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.12G>T
  hgvsp: ENSP00000389813.2:p.Arg4Ser
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg4Ser
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

12-112130537-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130537
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130537
    reference: chr 12
allele count: 1
allele frequency: 8.261185645363822e-6
allele num: 121048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.24G>C
  hgvsp: ENSP00000446959.1:p.Gln8His
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.24G>C
  hgvsp: ENSP00000446998.1:p.Gln8His
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.209G>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.196G>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.24G>C
  hgvsp: ENSP00000389813.2:p.Gln8His
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.24G>C
  hgvsp: ENSP00000421527.1:p.Gln8His
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.24G>C
  hgvsp: ENSP00000325137.4:p.Gln8His
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-989G>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.209G>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.221G>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6494G>C
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4818
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln8His
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum

12-112130543-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130543
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130543
    reference: chr 12
allele count: 3
allele frequency: 2.474716644944154e-5
allele num: 121226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.202C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.30C>T
  hgvsp: ENST00000552965.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.227C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.30C>T
  hgvsp: ENST00000313698.4:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.30C>T
  hgvsp: ENST00000455480.2:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.30C>T
  hgvsp: ENST00000549590.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.30C>T
  hgvsp: ENST00000514615.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6500C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.215C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.215C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-983C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro10Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-112130544-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130544
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130544
    reference: chr 12
allele count: 4
allele frequency: 3.299458888742246e-5
allele num: 121232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.31C>T
  hgvsp: ENSP00000446998.1:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.31C>T
  hgvsp: ENSP00000421527.1:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.216C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.216C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.31C>T
  hgvsp: ENSP00000325137.4:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-982C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.31C>T
  hgvsp: ENSP00000446959.1:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.228C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.203C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.31C>T
  hgvsp: ENSP00000389813.2:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6501C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg11Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

12-112130545-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130545
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130545
    reference: chr 12
allele count: 8
allele frequency: 6.597720487571544e-5
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.32G>A
  hgvsp: ENSP00000421527.1:p.Arg11His
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.229G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.32G>A
  hgvsp: ENSP00000446959.1:p.Arg11His
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.32G>A
  hgvsp: ENSP00000325137.4:p.Arg11His
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.32G>A
  hgvsp: ENSP00000389813.2:p.Arg11His
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.217G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6502G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-981G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.32G>A
  hgvsp: ENSP00000446998.1:p.Arg11His
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.217G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.204G>A
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg11His
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: G
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

12-112130553-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130553
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130553
    reference: chr 12
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6510T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.40T>C
  hgvsp: ENSP00000421527.1:p.Trp14Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.225T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.225T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.40T>C
  hgvsp: ENSP00000325137.4:p.Trp14Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.40T>C
  hgvsp: ENSP00000446959.1:p.Trp14Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.40T>C
  hgvsp: ENSP00000389813.2:p.Trp14Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-973T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446998
  ensembl transcript: ENST00000552965
  gene symbol: ACAD10
  hgvsc: ENST00000552965.1:c.40T>C
  hgvsp: ENST00000552965.1:c.40T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.237T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.212T>C
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp14Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

12-112130556-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130556
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130556
    reference: chr 12
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.43G>A
  hgvsp: ENSP00000325137.4:p.Val15Met
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.215G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.43G>A
  hgvsp: ENSP00000446959.1:p.Val15Met
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.43G>A
  hgvsp: ENSP00000389813.2:p.Val15Met
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.43G>A
  hgvsp: ENSP00000421527.1:p.Val15Met
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-970G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.228G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.228G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.240G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6513G>A
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1693
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val15Met
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

12-112130556-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130556
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130556
    reference: chr 12
allele count: 2
allele frequency: 1.648179585647652e-5
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6513G>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.240G>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.43G>C
  hgvsp: ENSP00000389813.2:p.Val15Leu
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.43G>C
  hgvsp: ENSP00000446959.1:p.Val15Leu
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.43G>C
  hgvsp: ENSP00000421527.1:p.Val15Leu
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.228G>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.228G>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.43G>C
  hgvsp: ENSP00000325137.4:p.Val15Leu
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.215G>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-970G>C
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22556
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3060
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val15Leu
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

12-112130557-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130557
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130557
    reference: chr 12
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.216T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-969T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.44T>G
  hgvsp: ENSP00000446959.1:p.Val15Gly
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.44T>G
  hgvsp: ENSP00000389813.2:p.Val15Gly
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6514T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.229T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.229T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.44T>G
  hgvsp: ENSP00000325137.4:p.Val15Gly
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.241T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.44T>G
  hgvsp: ENSP00000421527.1:p.Val15Gly
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8218
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16983
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22556
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val15Gly
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

12-112130558-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130558
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130558
    reference: chr 12
allele count: 2
allele frequency: 1.648125257519571e-5
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.230G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.45G>A
  hgvsp: ENST00000549590.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.242G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.45G>A
  hgvsp: ENST00000313698.4:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.230G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-968G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.45G>A
  hgvsp: ENST00000514615.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.45G>A
  hgvsp: ENST00000455480.2:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6515G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.217G>A
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15250
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3425
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22548
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val15Val
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

12-112130564-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130564
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130564
    reference: chr 12
allele count: 629
allele frequency: 5.182756006723575e-3
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.51A>G
  hgvsp: ENST00000313698.4:c.51A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.236A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.51A>G
  hgvsp: ENST00000549590.1:c.51A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.223A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-962A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.51A>G
  hgvsp: ENST00000455480.2:c.51A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6521A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.51A>G
  hgvsp: ENST00000514615.1:c.51A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.248A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.236A>G
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 12267
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 9.75e1
  variant carriers: 376
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 16976
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8224
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 6.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg17Arg
num of homozygotes: 23
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

12-112130568-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130568
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130568
    reference: chr 12
allele count: 2
allele frequency: 1.647962294622699e-5
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6525G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.55G>A
  hgvsp: ENSP00000446959.1:p.Ala19Thr
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.55G>A
  hgvsp: ENSP00000325137.4:p.Ala19Thr
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.227G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.252G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.240G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-958G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.55G>A
  hgvsp: ENSP00000389813.2:p.Ala19Thr
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.240G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.55G>A
  hgvsp: ENSP00000421527.1:p.Ala19Thr
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15271
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala19Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

12-112130570-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130570
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130570
    reference: chr 12
allele count: 7
allele frequency: 5.767202741892961e-5
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.254C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.57C>G
  hgvsp: ENST00000313698.4:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.57C>G
  hgvsp: ENST00000549590.1:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.242C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.242C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.229C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.57C>G
  hgvsp: ENST00000455480.2:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6527C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.57C>G
  hgvsp: ENST00000514615.1:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-956C>G
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1688
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala19Ala
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/12-112130578-AAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130578
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130576
    reference: chr 12
allele count: 4
allele frequency: 3.295327225993541e-5
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.255_256delAC
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-943_-942delAC
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.70_71delAC
  hgvsp: ENSP00000389813.2:p.Thr24ProfsTer60
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.242_243delAC
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.70_71delAC
  hgvsp: ENSP00000325137.4:p.Thr24ProfsTer60
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6540_-108+6541delAC
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.267_268delAC
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.70_71delAC
  hgvsp: ENSP00000446959.1:p.Thr24ProfsTer60
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.255_256delAC
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.70_71delAC
  hgvsp: ENSP00000421527.1:p.Thr24ProfsTer60
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16981
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr24ProfsTer60
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: AAC
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

12-112130579-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130579
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130579
    reference: chr 12
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: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.263A>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.238A>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.66A>T
  hgvsp: ENSP00000325137.4:p.Lys22Asn
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.251A>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.66A>T
  hgvsp: ENSP00000446959.1:p.Lys22Asn
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-947A>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.66A>T
  hgvsp: ENSP00000421527.1:p.Lys22Asn
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.66A>T
  hgvsp: ENSP00000389813.2:p.Lys22Asn
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6536A>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.251A>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7773
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys22Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum

12-112130582-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130582
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130582
    reference: chr 12
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.69C>T
  hgvsp: ENST00000313698.4:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.266C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-944C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.254C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.69C>T
  hgvsp: ENST00000455480.2:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.241C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.69C>T
  hgvsp: ENST00000549590.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6539C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.254C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.69C>T
  hgvsp: ENST00000514615.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7773
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22600
  bin: 6.25e1
  variant carriers: 0
hgvs: p.His23His
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

12-112130584-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130584
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130584
    reference: chr 12
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.256C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6541C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.71C>T
  hgvsp: ENSP00000421527.1:p.Thr24Ile
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.268C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-942C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.71C>T
  hgvsp: ENSP00000389813.2:p.Thr24Ile
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.256C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.71C>T
  hgvsp: ENSP00000325137.4:p.Thr24Ile
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.243C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.71C>T
  hgvsp: ENSP00000446959.1:p.Thr24Ile
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr24Ile
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

12-112130585-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130585
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130585
    reference: chr 12
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-941C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.72C>T
  hgvsp: ENST00000514615.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.257C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.72C>T
  hgvsp: ENST00000455480.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.72C>T
  hgvsp: ENST00000549590.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.269C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.257C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.72C>T
  hgvsp: ENST00000313698.4:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.244C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6542C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr24Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

12-112130586-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130586
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130586
    reference: chr 12
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.73C>T
  hgvsp: ENSP00000325137.4:p.Gln25Ter
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.258C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.245C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6543C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.73C>T
  hgvsp: ENSP00000389813.2:p.Gln25Ter
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.73C>T
  hgvsp: ENSP00000421527.1:p.Gln25Ter
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-940C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.73C>T
  hgvsp: ENSP00000446959.1:p.Gln25Ter
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.270C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.258C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3420
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln25Ter
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

12-112130589-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130589
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130589
    reference: chr 12
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.76C>T
  hgvsp: ENSP00000446959.1:p.Arg26Cys
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.76C>T
  hgvsp: ENSP00000421527.1:p.Arg26Cys
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-937C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.248C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6546C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.76C>T
  hgvsp: ENSP00000389813.2:p.Arg26Cys
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.273C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.261C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.76C>T
  hgvsp: ENSP00000325137.4:p.Arg26Cys
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.261C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7778
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg26Cys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

12-112130590-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130590
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130590
    reference: chr 12
allele count: 4
allele frequency: 3.295381522795802e-5
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.77G>A
  hgvsp: ENSP00000446959.1:p.Arg26His
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.77G>A
  hgvsp: ENSP00000325137.4:p.Arg26His
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-936G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.262G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.262G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6547G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.249G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.77G>A
  hgvsp: ENSP00000421527.1:p.Arg26His
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.77G>A
  hgvsp: ENSP00000389813.2:p.Arg26His
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.274G>A
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3056
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg26His
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

12-112130591-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130591
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130591
    reference: chr 12
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.78C>T
  hgvsp: ENST00000455480.2:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.78C>T
  hgvsp: ENST00000313698.4:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6548C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.78C>T
  hgvsp: ENST00000514615.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.263C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.250C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-935C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.275C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.78C>T
  hgvsp: ENST00000549590.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.263C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4211
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg26Arg
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

12-112130595-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130595
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130595
    reference: chr 12
allele count: 13
allele frequency: 1.071051937780121e-4
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.267C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.279C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.267C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.82C>T
  hgvsp: ENSP00000389813.2:p.His28Tyr
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6552C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.82C>T
  hgvsp: ENSP00000446959.1:p.His28Tyr
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-931C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.254C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.82C>T
  hgvsp: ENSP00000421527.1:p.His28Tyr
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.82C>T
  hgvsp: ENSP00000325137.4:p.His28Tyr
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15261
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His28Tyr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ

12-112130599-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130599
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130599
    reference: chr 12
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.86A>G
  hgvsp: ENSP00000325137.4:p.Gln29Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.86A>G
  hgvsp: ENSP00000389813.2:p.Gln29Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.271A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.86A>G
  hgvsp: ENSP00000446959.1:p.Gln29Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6556A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.271A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.86A>G
  hgvsp: ENSP00000421527.1:p.Gln29Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-927A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.258A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.283A>G
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2598
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln29Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

12-112130601-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130601
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130601
    reference: chr 12
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.273G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.88G>A
  hgvsp: ENSP00000421527.1:p.Gly30Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.88G>A
  hgvsp: ENSP00000389813.2:p.Gly30Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.260G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.88G>A
  hgvsp: ENSP00000446959.1:p.Gly30Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-925G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6558G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.273G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.285G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.88G>A
  hgvsp: ENSP00000325137.4:p.Gly30Arg
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1686
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3058
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly30Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS

12-112130603-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130603
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130603
    reference: chr 12
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.90G>A
  hgvsp: ENST00000313698.4:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6560G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.90G>A
  hgvsp: ENST00000455480.2:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.275G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.275G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.90G>A
  hgvsp: ENST00000514615.1:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-923G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.90G>A
  hgvsp: ENST00000549590.1:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.262G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.287G>A
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly30Gly
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

12-112130610-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130610
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130610
    reference: chr 12
allele count: 58
allele frequency: 4.779011898091691e-4
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.282C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.97C>T
  hgvsp: ENSP00000421527.1:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.97C>T
  hgvsp: ENSP00000389813.2:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.269C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.294C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-916C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6567C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.97C>T
  hgvsp: ENSP00000446959.1:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.282C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.97C>T
  hgvsp: ENSP00000325137.4:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 9.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4204
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg33Ter
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

12-112130611-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130611
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130611
    reference: chr 12
allele count: 28
allele frequency: 2.307071173145692e-4
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.98G>A
  hgvsp: ENSP00000325137.4:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.283G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.98G>A
  hgvsp: ENSP00000421527.1:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-915G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.270G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.98G>A
  hgvsp: ENSP00000446959.1:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.98G>A
  hgvsp: ENSP00000389813.2:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6568G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.283G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.295G>A
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16993
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7137
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22653
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1686
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg33Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-112130617-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130617
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130617
    reference: chr 12
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.289C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.301C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.104C>T
  hgvsp: ENSP00000389813.2:p.Thr35Ile
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.276C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6574C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.104C>T
  hgvsp: ENSP00000325137.4:p.Thr35Ile
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.104C>T
  hgvsp: ENSP00000446959.1:p.Thr35Ile
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-909C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.289C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.104C>T
  hgvsp: ENSP00000421527.1:p.Thr35Ile
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.75e1
  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: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1688
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3421
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr35Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

12-112130630-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130630
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130630
    reference: chr 12
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.302C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.117C>T
  hgvsp: ENST00000514615.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.289C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.302C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.117C>T
  hgvsp: ENST00000455480.2:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.117C>T
  hgvsp: ENST00000549590.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.117C>T
  hgvsp: ENST00000313698.4:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-896C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.314C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6587C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1688
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7767
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly39Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

12-112130633-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130633
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130633
    reference: chr 12
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.317C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.120C>T
  hgvsp: ENST00000514615.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.120C>T
  hgvsp: ENST00000455480.2:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-893C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.120C>T
  hgvsp: ENST00000313698.4:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.120C>T
  hgvsp: ENST00000549590.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6590C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.292C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.305C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.305C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12267
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22656
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser40Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

12-112130636-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130636
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130636
    reference: chr 12
allele count: 3
allele frequency: 2.472350876036327e-5
allele num: 121342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.308C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.320C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.123C>G
  hgvsp: ENST00000455480.2:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.308C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-890C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6593C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.123C>G
  hgvsp: ENST00000549590.1:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.123C>G
  hgvsp: ENST00000514615.1:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.295C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.123C>G
  hgvsp: ENST00000313698.4:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr41Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ

12-112130643-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130643
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130643
    reference: chr 12
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-883G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6600G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.302G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.327G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.130G>T
  hgvsp: ENSP00000325137.4:p.Ala44Ser
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.130G>T
  hgvsp: ENSP00000389813.2:p.Ala44Ser
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.130G>T
  hgvsp: ENSP00000421527.1:p.Ala44Ser
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.315G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.130G>T
  hgvsp: ENSP00000446959.1:p.Ala44Ser
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.315G>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16998
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8220
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7758
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3416
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala44Ser
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

12-112130645-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130645
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130645
    reference: chr 12
allele count: 46
allele frequency: 3.791938010056879e-4
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.132G>A
  hgvsp: ENST00000455480.2:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.132G>A
  hgvsp: ENST00000514615.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6602G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.317G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.132G>A
  hgvsp: ENST00000313698.4:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-881G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.132G>A
  hgvsp: ENST00000549590.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.317G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.329G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.304G>A
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 9.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15235
  bin: 9.75e1
  variant carriers: 46
genotype quality: GenotypeQuality
  all individuals: 4204
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala44Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

12-112130646-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130646
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130646
    reference: chr 12
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.133G>T
  hgvsp: ENSP00000421527.1:p.Val45Leu
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.133G>T
  hgvsp: ENSP00000446959.1:p.Val45Leu
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.305G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.133G>T
  hgvsp: ENSP00000389813.2:p.Val45Leu
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.318G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-880G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.330G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.318G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6603G>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.133G>T
  hgvsp: ENSP00000325137.4:p.Val45Leu
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4203
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2598
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val45Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

12-112130647-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130647
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130646
    reference: chr 12
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.307delG
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.320delG
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.135delG
  hgvsp: ENSP00000446959.1:p.Ile46PhefsTer31
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.135delG
  hgvsp: ENSP00000389813.2:p.Ile46PhefsTer31
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-878delG
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.320delG
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6605delG
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.332delG
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.135delG
  hgvsp: ENSP00000421527.1:p.Ile46PhefsTer31
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.135delG
  hgvsp: ENSP00000325137.4:p.Ile46PhefsTer31
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22640
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile46PhefsTer31
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
reference allele: TG
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

12-112130652-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130652
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130652
    reference: chr 12
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.139T>C
  hgvsp: ENSP00000446959.1:p.Phe47Leu
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-874T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.324T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.139T>C
  hgvsp: ENSP00000325137.4:p.Phe47Leu
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.139T>C
  hgvsp: ENSP00000389813.2:p.Phe47Leu
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.139T>C
  hgvsp: ENSP00000421527.1:p.Phe47Leu
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.336T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.324T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.311T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6609T>C
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2597
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Phe47Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

12-112130655-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130655
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130655
    reference: chr 12
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6612G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.327G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.142G>A
  hgvsp: ENSP00000446959.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.314G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-871G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.142G>A
  hgvsp: ENSP00000325137.4:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.327G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.142G>A
  hgvsp: ENSP00000389813.2:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.339G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.142G>A
  hgvsp: ENSP00000421527.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22525
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp48Asn
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

12-112130658-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130658
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130658
    reference: chr 12
allele count: 2
allele frequency: 1.649484536082474e-5
allele num: 121250
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-868A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.317A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6615A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.342A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.145A>G
  hgvsp: ENSP00000389813.2:p.Met49Val
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.145A>G
  hgvsp: ENSP00000325137.4:p.Met49Val
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.330A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.330A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.145A>G
  hgvsp: ENSP00000446959.1:p.Met49Val
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.145A>G
  hgvsp: ENSP00000421527.1:p.Met49Val
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7756
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Met49Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

12-112130659-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130659
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130659
    reference: chr 12
allele count: 4
allele frequency: 3.299567756623883e-5
allele num: 121228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.318T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.331T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.146T>G
  hgvsp: ENSP00000389813.2:p.Met49Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-867T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.146T>G
  hgvsp: ENSP00000421527.1:p.Met49Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.146T>G
  hgvsp: ENSP00000446959.1:p.Met49Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6616T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.331T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.343T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.146T>G
  hgvsp: ENSP00000325137.4:p.Met49Arg
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3415
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Met49Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

12-112130663-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130663
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130663
    reference: chr 12
allele count: 2
allele frequency: 1.650301179965344e-5
allele num: 121190
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.335C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6620C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.150C>T
  hgvsp: ENST00000313698.4:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.347C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.335C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.150C>T
  hgvsp: ENST00000455480.2:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.150C>T
  hgvsp: ENST00000549590.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.150C>T
  hgvsp: ENST00000514615.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-863C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.322C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7146
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3412
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly50Gly
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

12-112130664-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130664
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130664
    reference: chr 12
allele count: 1
allele frequency: 8.251914444151043e-6
allele num: 121184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.323G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-862G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.151G>A
  hgvsp: ENSP00000446959.1:p.Gly51Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.348G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.151G>A
  hgvsp: ENSP00000389813.2:p.Gly51Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.151G>A
  hgvsp: ENSP00000325137.4:p.Gly51Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.336G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.151G>A
  hgvsp: ENSP00000421527.1:p.Gly51Arg
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.336G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6621G>A
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly51Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

12-112130666-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130666
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130666
    reference: chr 12
allele count: 628
allele frequency: 5.183057673896537e-3
allele num: 121164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6623A>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.350A>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.153A>T
  hgvsp: ENST00000514615.1:c.153A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-860A>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.325A>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.153A>T
  hgvsp: ENST00000455480.2:c.153A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.338A>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.153A>T
  hgvsp: ENST00000313698.4:c.153A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.153A>T
  hgvsp: ENST00000549590.1:c.153A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.338A>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 12246
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8088
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 6.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 9.75e1
  variant carriers: 400
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 7137
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 16956
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2597
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly51Gly
num of homozygotes: 23
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

12-112130666-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130666
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130666
    reference: chr 12
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.153A>G
  hgvsp: ENST00000313698.4:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.153A>G
  hgvsp: ENST00000455480.2:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.338A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.153A>G
  hgvsp: ENST00000514615.1:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.338A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6623A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.350A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.153A>G
  hgvsp: ENST00000549590.1:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-860A>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.325A>G
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7137
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3412
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly51Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

12-112130672-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130672
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130672
    reference: chr 12
allele count: 1
allele frequency: 8.259820927082301e-6
allele num: 121068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.344C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.159C>T
  hgvsp: ENST00000313698.4:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.159C>T
  hgvsp: ENST00000514615.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.356C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-854C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.159C>T
  hgvsp: ENST00000549590.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6629C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.331C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.159C>T
  hgvsp: ENST00000455480.2:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.344C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7768
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu53Leu
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

12-112130674-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130674
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130674
    reference: chr 12
allele count: 9
allele frequency: 7.435435633912196e-5
allele num: 121042
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.346T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.161T>G
  hgvsp: ENSP00000389813.2:p.Ile54Ser
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.333T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.358T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.346T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6631T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-852T>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.161T>G
  hgvsp: ENSP00000421527.1:p.Ile54Ser
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.161T>G
  hgvsp: ENSP00000325137.4:p.Ile54Ser
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.161T>G
  hgvsp: ENSP00000446959.1:p.Ile54Ser
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4821
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17090
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4221
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile54Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

12-112130678-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130678
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130678
    reference: chr 12
allele count: 1
allele frequency: 8.266922390132602e-6
allele num: 120964
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.350T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-848T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.337T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6635T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.165T>C
  hgvsp: ENST00000514615.1:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.362T>C
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.165T>C
  hgvsp: ENST00000313698.4:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.165T>C
  hgvsp: ENST00000455480.2:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.165T>C
  hgvsp: ENST00000549590.1:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.350T>C
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22411
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro55Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

12-112130693-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130693
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130693
    reference: chr 12
allele count: 2
allele frequency: 1.6627315353663e-5
allele num: 120284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.365C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.180C>G
  hgvsp: ENST00000549590.1:c.180C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.352C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.180C>G
  hgvsp: ENST00000455480.2:c.180C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.180C>G
  hgvsp: ENST00000313698.4:c.180C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.180C>G
  hgvsp: ENST00000514615.1:c.180C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.365C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-833C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.377C>G
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6650C>G
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7193
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1695
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val60Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-112130693-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130693
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130693
    reference: chr 12
allele count: 2
allele frequency: 1.6627315353663e-5
allele num: 120284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.180C>T
  hgvsp: ENST00000549590.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.180C>T
  hgvsp: ENST00000313698.4:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6650C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.365C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.352C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.365C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.180C>T
  hgvsp: ENST00000514615.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.180C>T
  hgvsp: ENST00000455480.2:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.377C>T
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-833C>T
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val60Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

12-112130694-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130694
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130694
    reference: chr 12
allele count: 3
allele frequency: 2.49617253544565e-5
allele num: 120184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6651G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.366G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.366G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.181G>A
  hgvsp: ENSP00000446959.1:p.Ala61Thr
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.181G>A
  hgvsp: ENSP00000421527.1:p.Ala61Thr
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.181G>A
  hgvsp: ENSP00000389813.2:p.Ala61Thr
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.353G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.181G>A
  hgvsp: ENSP00000325137.4:p.Ala61Thr
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-832G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.378G>A
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4818
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3036
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala61Thr
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

12-112130700-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 112130700
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 112130700
    reference: chr 12
allele count: 1
allele frequency: 8.346827370916315e-6
allele num: 119806
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000325137
  ensembl transcript: ENST00000313698
  gene symbol: ACAD10
  hgvsc: ENST00000313698.4:c.187G>A
  hgvsp: ENSP00000325137.4:p.Glu63Lys
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000509936
  gene symbol: ACAD10
  hgvsc: ENST00000509936.1:n.372G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000446959
  ensembl transcript: ENST00000549590
  gene symbol: ACAD10
  hgvsc: ENST00000549590.1:c.187G>A
  hgvsp: ENSP00000446959.1:p.Glu63Lys
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000449097
  ensembl transcript: ENST00000515283
  gene symbol: ACAD10
  hgvsc: ENST00000515283.1:c.-108+6657G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000511915
  gene symbol: ACAD10
  hgvsc: ENST00000511915.1:n.384G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000421527
  ensembl transcript: ENST00000514615
  gene symbol: ACAD10
  hgvsc: ENST00000514615.1:c.187G>A
  hgvsp: ENSP00000421527.1:p.Glu63Lys
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000376411
  ensembl transcript: ENST00000392636
  gene symbol: ACAD10
  hgvsc: ENST00000392636.2:c.-826G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111271
  ensembl protein: ENSP00000389813
  ensembl transcript: ENST00000455480
  gene symbol: ACAD10
  hgvsc: ENST00000455480.2:c.187G>A
  hgvsp: ENSP00000389813.2:p.Glu63Lys
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000507135
  gene symbol: ACAD10
  hgvsc: ENST00000507135.1:n.359G>A
  variant of: http://identifiers.org/hgnc/21597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111271
  ensembl transcript: ENST00000413681
  gene symbol: ACAD10
  hgvsc: ENST00000413681.3:n.372G>A
  variant of: http://identifiers.org/hgnc/21597
canonical: true
consequence: missense
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 7178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu63Lys
num of homozygotes: 0
reference allele: G

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23050
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2448
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.407e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.19e0

DP
type: SiteQuality
SIO_000300: 4.68463e5

FS
type: SiteQuality
SIO_000300: 1.838e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

GenotypeQuality
all individuals: 393
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3453
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16368
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1708
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4261
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3009
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15483
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 529
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7239
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2614
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.680389850445303e-4
allele num: 11902
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e-1

QD
type: SiteQuality
SIO_000300: 1.434e1

MQRankSum
type: SiteQuality
SIO_000300: 3.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.32e0

FS
type: SiteQuality
SIO_000300: 7.17e-1

DP
type: SiteQuality
SIO_000300: 2.088676e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

GenotypeQuality
all individuals: 917
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16368
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2614
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3009
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15483
bin: 9.75e1
variant carriers: 425

GenotypeQuality
all individuals: 7239
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3453
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4261
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1708
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 7
allele frequency: 6.08378237441335e-4
allele num: 11506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.940617116242965e-4
allele num: 10306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 116
allele frequency: 1.754385964912281e-2
allele num: 6612
num of homozygotes: 1

South Asian
type: Population
allele count: 9
allele frequency: 7.561754327003865e-4
allele num: 11902
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.196172248803828e-3
allele num: 836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 292
allele frequency: 4.499090937105174e-3
allele num: 64902
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.32e0

FS
type: SiteQuality
SIO_000300: 7.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e-1

QD
type: SiteQuality
SIO_000300: 1.434e1

DP
type: SiteQuality
SIO_000300: 2.088676e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 182
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17036
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7361
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1859
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 616
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3444
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4240
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2618
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3030
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.081189339084887e-5
allele num: 64910
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.300000000000001e0

FS
type: SiteQuality
SIO_000300: 1.633e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQ
type: SiteQuality
SIO_000300: 5.904e1

DP
type: SiteQuality
SIO_000300: 2.084823e6

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.64e-1

GenotypeQuality
all individuals: 7367
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2620
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 203
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17071
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1700
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4223
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15124
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3430
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11920
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540594669542443e-5
allele num: 64910
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.69e-1

FS
type: SiteQuality
SIO_000300: 1.6726e1

QD
type: SiteQuality
SIO_000300: 1.44e1

MQ
type: SiteQuality
SIO_000300: 5.745e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.409e0

DP
type: SiteQuality
SIO_000300: 2.085179e6

GenotypeQuality
all individuals: 153
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2621
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.25e1
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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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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15126
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 1
allele frequency: 9.701202949165696e-5
allele num: 10308
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64942
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12012
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

QD
type: SiteQuality
SIO_000300: 1.242e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

VQSLOD
type: SiteQuality
SIO_000300: 6.03e-1

FS
type: SiteQuality
SIO_000300: 1.226e0

DP
type: SiteQuality
SIO_000300: 2.088882e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.51e-1

GenotypeQuality
all individuals: 437
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 2.5e0
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15128
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3027
bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12138
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539029795616843e-5
allele num: 64976
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.615e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-1

QD
type: SiteQuality
SIO_000300: 1.194e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

FS
type: SiteQuality
SIO_000300: 5.407e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-1

DP
type: SiteQuality
SIO_000300: 2.091057e6

MQ
type: SiteQuality
SIO_000300: 5.893e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

GenotypeQuality
all individuals: 131
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 688
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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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bin: 7.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4198
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
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: 1
allele frequency: 9.686168151879117e-5
allele num: 10324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65086
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12400
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.961e0

QD
type: SiteQuality
SIO_000300: 1.159e1

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.11e-1

FS
type: SiteQuality
SIO_000300: 2.834e0

MQ
type: SiteQuality
SIO_000300: 5.88e1

DP
type: SiteQuality
SIO_000300: 2.096182e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

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

GenotypeQuality
all individuals: 3031
bin: 7.25e1
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: 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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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12536
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.935359009096187e-4
allele num: 10334
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.097822e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.394e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.97e-1

FS
type: SiteQuality
SIO_000300: 1.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

VQSLOD
type: SiteQuality
SIO_000300: -1.979e0

QD
type: SiteQuality
SIO_000300: 1.657e1

MQRankSum
type: SiteQuality
SIO_000300: 2.94e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
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GenotypeQuality
all individuals: 189
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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: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2620
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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: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3031
bin: 7.25e1
variant carriers: 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: 10340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533036946190403e-5
allele num: 65230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12800
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.491e0

QD
type: SiteQuality
SIO_000300: 1.223e1

FS
type: SiteQuality
SIO_000300: 1.041e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.33e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.043e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: -5.45e-1

DP
type: SiteQuality
SIO_000300: 2.102285e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12934
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.401e1

ReadPosRankSum
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BaseQRankSum
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SIO_000300: -6.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.24e-1

DP
type: SiteQuality
SIO_000300: 2.105733e6

MQRankSum
type: SiteQuality
SIO_000300: 1.14e-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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variant carriers: 604

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2594
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 37
allele frequency: 3.205683590365621e-3
allele num: 11542
num of homozygotes: 0

African
type: Population
allele count: 571
allele frequency: 5.520108275328693e-2
allele num: 10344
num of homozygotes: 21

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

Other
type: Population
allele count: 2
allele frequency: 2.347417840375587e-3
allele num: 852
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.143294549908144e-4
allele num: 65320
num of homozygotes: 1

South Asian
type: Population
allele count: 3
allele frequency: 2.299202942979767e-4
allele num: 13048
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 2.914e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

MQRankSum
type: SiteQuality
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DP
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SIO_000300: 2.125255e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.28e-2

QD
type: SiteQuality
SIO_000300: 1.45e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.97e-1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 114
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variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 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: 10356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527417137620284e-5
allele num: 65470
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13514
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.356e0

MQRankSum
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SIO_000300: 3.79e-1

InbreedingCoeff
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SIO_000300: 3.1e-3

ReadPosRankSum
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SIO_000300: -7.97e-1

QD
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VQSLOD
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MQ
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SIO_000300: 5.97e1

ClippingRankSum
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SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 2.131553e6

BaseQRankSum
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SIO_000300: -1.985e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 12
allele frequency: 1.832956558929553e-4
allele num: 65468
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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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: 858
num of homozygotes: 0

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

VQSLOD
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MQRankSum
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FS
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InbreedingCoeff
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DP
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ClippingRankSum
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 6.32e-1

BaseQRankSum
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SIO_000300: 1.36e0

QD
type: SiteQuality
SIO_000300: 1.215e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14008
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65608
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: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

Other
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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: 8642
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QD
type: SiteQuality
SIO_000300: 1.177e1

VQSLOD
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BaseQRankSum
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SIO_000300: -3.171e0

MQ
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SIO_000300: 5.912e1

MQRankSum
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SIO_000300: -8.93e-1

FS
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SIO_000300: 0.0e0

DP
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SIO_000300: 2.139127e6

InbreedingCoeff
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SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.61e-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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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515289268721399e-5
allele num: 65994
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10392
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: 886
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.153428e6

ClippingRankSum
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SIO_000300: -1.536e0

QD
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SIO_000300: 1.169e1

MQRankSum
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SIO_000300: -4.66e-1

VQSLOD
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SIO_000300: -5.635e-1

FS
type: SiteQuality
SIO_000300: 2.729e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
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SIO_000300: -3.309e0

ReadPosRankSum
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SIO_000300: 2.79e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

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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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: 8650
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66120
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.564264145989234e-5
allele num: 15234
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African
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

InbreedingCoeff
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DP
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SIO_000300: 2.15868e6

MQRankSum
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ClippingRankSum
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SIO_000300: -3.3e-1

MQ
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VQSLOD
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QD
type: SiteQuality
SIO_000300: 4.59e0

FS
type: SiteQuality
SIO_000300: 1.4903e1

BaseQRankSum
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SIO_000300: 4.47e0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510026576467746e-5
allele num: 66224
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
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DP
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ClippingRankSum
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VQSLOD
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FS
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QD
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BaseQRankSum
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InbreedingCoeff
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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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Other
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South Asian
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allele frequency: 6.300403225806451e-5
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.502900598154438e-5
allele num: 66538
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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DP
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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allele num: 66606
num of homozygotes: 0

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

East Asian
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European (Non-Finnish)
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allele frequency: 4.504098729844158e-5
allele num: 66606
num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 66670
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European (Finnish)
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African
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Latino
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South Asian
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Other
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ReadPosRankSum
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VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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FS
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MQ
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ClippingRankSum
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QD
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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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East Asian
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allele num: 8652
num of homozygotes: 0

African
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num of homozygotes: 0

European (Non-Finnish)
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Other
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Latino
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European (Finnish)
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South Asian
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BaseQRankSum
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MQRankSum
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VQSLOD
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DP
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ClippingRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQ
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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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African
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East Asian
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South 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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DP
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BaseQRankSum
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ReadPosRankSum
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FS
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QD
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MQ
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Non-Finnish)
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South Asian
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East Asian
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European (Finnish)
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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QD
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DP
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MQRankSum
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ReadPosRankSum
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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East Asian
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.769e0

QD
type: SiteQuality
SIO_000300: 1.475e1

MQRankSum
type: SiteQuality
SIO_000300: 4.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.76e0

DP
type: SiteQuality
SIO_000300: 2.183814e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

GenotypeQuality
all individuals: 4215
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22561
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2598
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3422
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15291
bin: 9.75e1
variant carriers: 606

GenotypeQuality
all individuals: 7773
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 38
allele frequency: 3.28208671618587e-3
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.099076406381192e-4
allele num: 66696
num of homozygotes: 1

African
type: Population
allele count: 572
allele frequency: 5.497885428681276e-2
allele num: 10404
num of homozygotes: 22

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.11e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.03e0

DP
type: SiteQuality
SIO_000300: 2.201797e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.571e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1687
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7779
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4215
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2598
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22572
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3422
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3056
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.211e0

VQSLOD
type: SiteQuality
SIO_000300: -1.121e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.200089e6

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.43e-1

QD
type: SiteQuality
SIO_000300: 1.406e1

MQ
type: SiteQuality
SIO_000300: 5.867e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.218e0

GenotypeQuality
all individuals: 7778
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15269
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 3422
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4216
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2599
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22578
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.495577609210566e-5
allele num: 66706
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-1

DP
type: SiteQuality
SIO_000300: 2.200241e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.908e0

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

MQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

QD
type: SiteQuality
SIO_000300: 1.402e1

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

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

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3420
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3057
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22601
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
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: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7773
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15265
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4217
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.99538355466291e-5
allele num: 66718
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.159e0

DP
type: SiteQuality
SIO_000300: 2.200128e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.09e-1

QD
type: SiteQuality
SIO_000300: 1.637e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.023e1

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3057
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22597
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1687
bin: 8.75e1
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: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3420
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4217
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2599
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15261
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.56e0

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.548e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

DP
type: SiteQuality
SIO_000300: 2.199802e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.18e1

MQ
type: SiteQuality
SIO_000300: 5.983e1

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1687
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4217
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3057
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3419
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2599
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15260
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
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: 11578
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.206e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.123e0

DP
type: SiteQuality
SIO_000300: 2.199956e6

FS
type: SiteQuality
SIO_000300: 6.634e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.58e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2599
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3420
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 22605
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7772
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4217
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3055
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15261
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1687
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.919e1

MQRankSum
type: SiteQuality
SIO_000300: 6.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.182e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.574e-1

FS
type: SiteQuality
SIO_000300: 7.81e-1

DP
type: SiteQuality
SIO_000300: 2.199962e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.589e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

QD
type: SiteQuality
SIO_000300: 1.132e1

GenotypeQuality
all individuals: 7773
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22606
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3056
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15261
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1687
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3421
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4216
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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African
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allele num: 10402
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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FS
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VQSLOD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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DP
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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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Latino
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num of homozygotes: 0

Other
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European (Non-Finnish)
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allele num: 66720
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African
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East Asian
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South Asian
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European (Finnish)
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ClippingRankSum
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InbreedingCoeff
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FS
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DP
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QD
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MQRankSum
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MQ
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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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South Asian
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European (Non-Finnish)
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allele frequency: 1.948499655265446e-4
allele num: 66718
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Latino
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European (Finnish)
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East Asian
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African
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Other
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ReadPosRankSum
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FS
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ClippingRankSum
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VQSLOD
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DP
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InbreedingCoeff
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BaseQRankSum
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QD
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MQRankSum
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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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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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Other
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South Asian
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Latino
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FS
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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QD
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DP
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InbreedingCoeff
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VQSLOD
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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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East Asian
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European (Non-Finnish)
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African
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Latino
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South Asian
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European (Finnish)
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MQ
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ClippingRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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FS
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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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South Asian
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Latino
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European (Finnish)
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.6e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

DP
type: SiteQuality
SIO_000300: 2.199732e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.929e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.41e1

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7774
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3057
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22642
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15261
bin: 9.75e1
variant carriers: 58

GenotypeQuality
all individuals: 2595
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3420
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1686
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 52
allele frequency: 6.010171058714748e-3
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49707690001499e-5
allele num: 66710
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.181e1

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

DP
type: SiteQuality
SIO_000300: 2.204868e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.26e-1

FS
type: SiteQuality
SIO_000300: 5.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.91e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.2e-1

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

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

GenotypeQuality
all individuals: 7775
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3058
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4207
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2596
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3422
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15244
bin: 9.75e1
variant carriers: 28

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 27
allele frequency: 4.047247871447416e-4
allele num: 66712
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.293e1

MQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.15e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.67e0

DP
type: SiteQuality
SIO_000300: 2.202724e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.52e-1

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

GenotypeQuality
all individuals: 5
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variant carriers: 0

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

GenotypeQuality
all individuals: 4211
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15223
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2597
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 7777
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22664
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
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: 10396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.033e1

MQRankSum
type: SiteQuality
SIO_000300: 6.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e-1

DP
type: SiteQuality
SIO_000300: 2.199775e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

FS
type: SiteQuality
SIO_000300: 1.204e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.66e-1

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 15222
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 4207
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 22658
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3058
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3417
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.199567e6

FS
type: SiteQuality
SIO_000300: 3.136e0

VQSLOD
type: SiteQuality
SIO_000300: 1.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.158e0

MQRankSum
type: SiteQuality
SIO_000300: -5.24e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.275e0

QD
type: SiteQuality
SIO_000300: 8.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.97e-1

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

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 3056
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2597
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 4207
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variant carriers: 0

GenotypeQuality
all individuals: 1688
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variant carriers: 0

GenotypeQuality
all individuals: 15223
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variant carriers: 1

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 7766
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3417
bin: 8.25e1
variant carriers: 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: 10388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.199467e6

MQ
type: SiteQuality
SIO_000300: 5.89e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

QD
type: SiteQuality
SIO_000300: 7.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

FS
type: SiteQuality
SIO_000300: 1.377e0

VQSLOD
type: SiteQuality
SIO_000300: -1.95e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.25e-1

GenotypeQuality
all individuals: 3416
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15224
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4209
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GenotypeQuality
all individuals: 3057
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GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 2597
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1688
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7760
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817520901490367e-4
allele num: 16506
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.199538e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.69e0

VQSLOD
type: SiteQuality
SIO_000300: 5.620000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.21e-1

FS
type: SiteQuality
SIO_000300: 2.362e0

QD
type: SiteQuality
SIO_000300: 1.116e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.46e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 70
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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
all individuals: 6
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15222
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variant carriers: 1

GenotypeQuality
all individuals: 4208
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.129999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.199117e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.774e0

QD
type: SiteQuality
SIO_000300: 1.016e1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: 2.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

FS
type: SiteQuality
SIO_000300: 1.775e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

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

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 22608
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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: 12
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3052
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.460207612456747e-4
allele num: 11560
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 34
allele frequency: 5.098368522072936e-4
allele num: 66688
num of homozygotes: 0

European (Finnish)
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allele count: 7
allele frequency: 1.058681185722928e-3
allele num: 6612
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.203478e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.1e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.65e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.79e-1

QD
type: SiteQuality
SIO_000300: 1.337e1

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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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7761
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

FS
type: SiteQuality
SIO_000300: 6.623e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQRankSum
type: SiteQuality
SIO_000300: 9.61e-1

DP
type: SiteQuality
SIO_000300: 2.198364e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.14e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3414
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.198297e6

QD
type: SiteQuality
SIO_000300: 1.546e1

FS
type: SiteQuality
SIO_000300: 8.169999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.046e1

VQSLOD
type: SiteQuality
SIO_000300: 2.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.075e0

GenotypeQuality
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bin: 2.5e0
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: 9
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e0

DP
type: SiteQuality
SIO_000300: 2.197878e6

MQ
type: SiteQuality
SIO_000300: 5.947e1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.6e0

QD
type: SiteQuality
SIO_000300: 1.657e1

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 127
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.925e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.45e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.348e0

VQSLOD
type: SiteQuality
SIO_000300: 4.1e-2

QD
type: SiteQuality
SIO_000300: 1.429e1

DP
type: SiteQuality
SIO_000300: 2.197531e6

GenotypeQuality
all individuals: 2597
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.118e0

DP
type: SiteQuality
SIO_000300: 2.197395e6

MQRankSum
type: SiteQuality
SIO_000300: -6.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.507e0

QD
type: SiteQuality
SIO_000300: 1.341e1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.00294144130624e-5
allele num: 66634
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.04e-1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.42e-1

VQSLOD
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.002191599867904e-5
allele num: 66618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
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Latino
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allele frequency: 0.0e0
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South Asian
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Other
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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DP
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MQRankSum
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InbreedingCoeff
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QD
type: SiteQuality
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.070171178827243e-5
allele num: 16474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.368e1

FS
type: SiteQuality
SIO_000300: 2.035e0

DP
type: SiteQuality
SIO_000300: 2.196377e6

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

GenotypeQuality
all individuals: 7734
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1685
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3050
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4196
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22456
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15222
bin: 9.75e1
variant carriers: 605

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3412
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 37
allele frequency: 3.202908587257618e-3
allele num: 11552
num of homozygotes: 0

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

African
type: Population
allele count: 572
allele frequency: 5.514847666795218e-2
allele num: 10372
num of homozygotes: 22

Other
type: Population
allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.821272462360369e-4
allele num: 16472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.102228362063788e-4
allele num: 66596
num of homozygotes: 1

DP
type: SiteQuality
SIO_000300: 2.206463e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.16e-2

FS
type: SiteQuality
SIO_000300: 5.570000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.287e0

VQSLOD
type: SiteQuality
SIO_000300: 4.67e0

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

QD
type: SiteQuality
SIO_000300: 1.383e1

GenotypeQuality
all individuals: 7734
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1685
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22456
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2597
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3050
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4196
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15222
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50159168718842e-5
allele num: 66596
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.287e0

VQSLOD
type: SiteQuality
SIO_000300: 4.67e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.16e-2

DP
type: SiteQuality
SIO_000300: 2.206463e6

FS
type: SiteQuality
SIO_000300: 5.570000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

QD
type: SiteQuality
SIO_000300: 1.383e1

GenotypeQuality
all individuals: 3074
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4220
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2621
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1697
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3441
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14824
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22537
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
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: 66548
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.084205402774397e-5
allele num: 16436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
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: 10364
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.42e0

QD
type: SiteQuality
SIO_000300: 1.42e1

MQ
type: SiteQuality
SIO_000300: 5.911e1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.159437e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.265e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e0

VQSLOD
type: SiteQuality
SIO_000300: -8.389e-1

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3440
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22545
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3075
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7761
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2618
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14827
bin: 9.75e1
variant carriers: 9

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
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: 9
allele frequency: 8.685581933989577e-4
allele num: 10362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66538
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e-1

FS
type: SiteQuality
SIO_000300: 5.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.468e1

DP
type: SiteQuality
SIO_000300: 2.159464e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.26e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
SIO_000300: -3.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.3e-2

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

GenotypeQuality
all individuals: 14821
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 388
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3066
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4217
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7756
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 80
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1696
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3441
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2618
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503668952243474e-5
allele num: 66504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-1

FS
type: SiteQuality
SIO_000300: 7.599e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 2.157687e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

QD
type: SiteQuality
SIO_000300: 1.167e1

MQRankSum
type: SiteQuality
SIO_000300: 7.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

GenotypeQuality
all individuals: 14826
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2615
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21287
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3438
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7644
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3039
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1077
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4188
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66226
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.243756243756244e-5
allele num: 16016
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e0

QD
type: SiteQuality
SIO_000300: 1.452e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.144776e6

FS
type: SiteQuality
SIO_000300: 4.904e0

VQSLOD
type: SiteQuality
SIO_000300: 8.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.07e-1

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

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

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

GenotypeQuality
all individuals: 139
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3039
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21287
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2615
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4188
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1695
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7644
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14826
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1077
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3438
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.663703131039814e-5
allele num: 10348
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66226
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.243756243756244e-5
allele num: 16016
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

FS
type: SiteQuality
SIO_000300: 4.904e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.07e-1

QD
type: SiteQuality
SIO_000300: 1.452e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e0

VQSLOD
type: SiteQuality
SIO_000300: 8.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-2

DP
type: SiteQuality
SIO_000300: 2.144776e6

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

GenotypeQuality
all individuals: 2615
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 148
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4183
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3437
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21150
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14825
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7622
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1695
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.933114247052001e-4
allele num: 10346
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15956
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66202
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.78e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.973e0

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.98e-1

QD
type: SiteQuality
SIO_000300: 1.399e1

DP
type: SiteQuality
SIO_000300: 2.142917e6

FS
type: SiteQuality
SIO_000300: 3.924e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0