1-6324738-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6324738
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6324738
    reference: chr 1
allele count: 1
allele frequency: 8.535627710061798e-6
allele num: 117156
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.909G>C
  hgvsp: ENSP00000367073.3:p.Glu303Asp
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.972G>C
  hgvsp: ENSP00000367076.3:p.Glu324Asp
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1032G>C
  hgvsp: ENSP00000354615.4:p.Glu344Asp
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.936G>C
  hgvsp: ENSP00000476610.1:p.Glu312Asp
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*360G>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1062G>C
  hgvsp: ENSP00000367086.2:p.Glu354Asp
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.717G>C
  hgvsp: ENSP00000439218.1:p.Glu239Asp
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*157G>C
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36766
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46809
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2549
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu354Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

1-6324741-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6324741
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6324741
    reference: chr 1
allele count: 20
allele frequency: 1.711889069588291e-4
allele num: 116830
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.969C>T
  hgvsp: ENST00000377845.3:c.969C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*357C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.906C>T
  hgvsp: ENST00000377842.3:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1059C>T
  hgvsp: ENST00000377855.2:c.1059C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.714C>T
  hgvsp: ENST00000545482.1:c.714C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.933C>T
  hgvsp: ENST00000608083.1:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1029C>T
  hgvsp: ENST00000361521.4:c.1029C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*154C>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36077
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14486
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2448
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2932
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp353Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

1-6324747-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6324747
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6324747
    reference: chr 1
allele count: 1446
allele frequency: 1.247132285719214e-2
allele num: 115946
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1053C>T
  hgvsp: ENST00000377855.2:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.900C>T
  hgvsp: ENST00000377842.3:c.900C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.708C>T
  hgvsp: ENST00000545482.1:c.708C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.963C>T
  hgvsp: ENST00000377845.3:c.963C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1023C>T
  hgvsp: ENST00000361521.4:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*148C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.927C>T
  hgvsp: ENST00000608083.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*351C>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 1.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 157
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 34150
  bin: 2.25e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 3.25e1
  variant carriers: 220
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.75e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 13977
  bin: 2.75e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 180
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3881
  bin: 2.25e1
  variant carriers: 1
hgvs: p.Thr351Thr
num of homozygotes: 19
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD

1-6324752-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6324752
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6324751
    reference: chr 1
allele count: 1
allele frequency: 8.695198511382016e-6
allele num: 115006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.921delC
  hgvsp: ENSP00000476610.1:p.Glu308ArgfsTer19
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1017delC
  hgvsp: ENSP00000354615.4:p.Glu340ArgfsTer19
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.957delC
  hgvsp: ENSP00000367076.3:p.Glu320ArgfsTer19
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*345delC
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.702delC
  hgvsp: ENSP00000439218.1:p.Glu235ArgfsTer19
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1047delC
  hgvsp: ENSP00000367086.2:p.Glu350ArgfsTer19
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*142delC
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.894delC
  hgvsp: ENSP00000367073.3:p.Glu299ArgfsTer19
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu350ArgfsTer19
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: CG
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

1-6324753-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6324753
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6324753
    reference: chr 1
allele count: 8
allele frequency: 6.967548642198959e-5
allele num: 114818
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.894C>T
  hgvsp: ENST00000377842.3:c.894C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.702C>T
  hgvsp: ENST00000545482.1:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.957C>T
  hgvsp: ENST00000377845.3:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1047C>T
  hgvsp: ENST00000377855.2:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1017C>T
  hgvsp: ENST00000361521.4:c.1017C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*345C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*142C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.921C>T
  hgvsp: ENST00000608083.1:c.921C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13884
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1047C>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

1-6324753-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6324753
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6324753
    reference: chr 1
allele count: 1
allele frequency: 8.709435802748698e-6
allele num: 114818
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*345C>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.957C>G
  hgvsp: ENST00000377845.3:c.957C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.702C>G
  hgvsp: ENST00000545482.1:c.702C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1017C>G
  hgvsp: ENST00000361521.4:c.1017C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1047C>G
  hgvsp: ENST00000377855.2:c.1047C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.921C>G
  hgvsp: ENST00000608083.1:c.921C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*142C>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.894C>G
  hgvsp: ENST00000377842.3:c.894C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13884
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1036
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42867
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 2.75e1
  variant carriers: 0
hgvs: c.1047C>G
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum

1-6324755-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6324755
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6324755
    reference: chr 1
allele count: 1
allele frequency: 8.736676568233443e-6
allele num: 114460
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1015C>G
  hgvsp: ENSP00000354615.4:p.Pro339Ala
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.892C>G
  hgvsp: ENSP00000367073.3:p.Pro298Ala
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*343C>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.955C>G
  hgvsp: ENSP00000367076.3:p.Pro319Ala
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.919C>G
  hgvsp: ENSP00000476610.1:p.Pro307Ala
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1045C>G
  hgvsp: ENSP00000367086.2:p.Pro349Ala
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*140C>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.700C>G
  hgvsp: ENSP00000439218.1:p.Pro234Ala
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro349Ala
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

1-6324765-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6324765
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6324765
    reference: chr 1
allele count: 2
allele frequency: 1.792821542543655e-5
allele num: 111556
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.955-10T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1045-10T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*140-10T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*343-10T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.700-10T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.892-10T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1015-10T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.919-10T>C
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10048
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2845
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33602
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2428
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

1-6324770-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6324770
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6324768
    reference: chr 1
allele count: 19
allele frequency: 1.72073393830716e-4
allele num: 110418
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.892-17_892-16delCT
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.955-17_955-16delCT
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1015-17_1015-16delCT
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*140-17_*140-16delCT
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*343-17_*343-16delCT
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.700-17_700-16delCT
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1045-17_1045-16delCT
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.919-17_919-16delCT
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12887
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22865
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11024
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3864
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3171
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29188
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11355
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1934
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: CAG
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-6324772-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6324772
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6324772
    reference: chr 1
allele count: 1
allele frequency: 9.061910975786574e-6
allele num: 110352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*140-17C>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1045-17C>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.892-17C>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.700-17C>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1015-17C>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.919-17C>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*343-17C>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.955-17C>A
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4726
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1891
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3833
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30751
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3174
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

1-6324782-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6324782
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6324782
    reference: chr 1
allele count: 1
allele frequency: 9.226113591910544e-6
allele num: 108388
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1045-27C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.700-27C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.892-27C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*140-27C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.919-27C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*343-27C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.955-27C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1015-27C>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4011
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6870
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-6324783-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6324783
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6324783
    reference: chr 1
allele count: 1
allele frequency: 9.245733094177037e-6
allele num: 108158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.919-28C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1015-28C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.892-28C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*140-28C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1045-28C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*343-28C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.700-28C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.955-28C>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15227
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4228
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4968
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-6324798-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6324798
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6324798
    reference: chr 1
allele count: 19
allele frequency: 1.838555475992336e-4
allele num: 103342
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1045-43C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1015-43C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.919-43C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*140-43C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.700-43C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*343-43C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.955-43C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.892-43C>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16102
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20136
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7343
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8627
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9342
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7855
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3141
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7352
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 939
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13955
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

1-6324803-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6324803
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6324803
    reference: chr 1
allele count: 30
allele frequency: 2.964895635673624e-4
allele num: 101184
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*140-48T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.955-48T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1045-48T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.700-48T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.892-48T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.919-48T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1015-48T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*343-48T>C
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8373
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19378
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9232
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15867
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7597
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3087
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2666
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2455
  bin: 9.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1039
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 8.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

1-6341111-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341111
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341111
    reference: chr 1
allele count: 1
allele frequency: 1.228531413548244e-5
allele num: 81398
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+51G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+51G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+51G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+51G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+51G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+51G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+51G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+51G>A
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10016
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2525
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1953
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2362
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2112
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8664
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11042
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-6341117-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341117
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341117
    reference: chr 1
allele count: 4
allele frequency: 4.865469761105434e-5
allele num: 82212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+45C>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+45C>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+45C>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+45C>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+45C>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+45C>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+45C>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+45C>G
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16318
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20252
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8359
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5633
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3052
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2428
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6322
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1659
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

1-6341133-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341133
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341133
    reference: chr 1
allele count: 1
allele frequency: 1.157997128167122e-5
allele num: 86356
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+29C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+29C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+29C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+29C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+29C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+29C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+29C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+29C>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15972
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD

1-6341135-G-GCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341135
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341137
    reference: chr 1
allele count: 12
allele frequency: 1.375547353217635e-4
allele num: 87238
alternate allele: GCT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+26_1014+27insAG
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+26_891+27insAG
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+26_954+27insAG
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+26_699+27insAG
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+26_1044+27insAG
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+26_*139+27insAG
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+26_*342+27insAG
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+26_918+27insAG
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16520
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5661
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15187
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15311
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2871
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/1-6341136-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341136
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341136
    reference: chr 1
allele count: 2
allele frequency: 2.272985566541652e-5
allele num: 87990
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+26G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+26G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+26G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+26G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+26G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+26G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+26G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+26G>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15073
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6256
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3040
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15516
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4577
  bin: 2.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

1-6341136-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341136
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341136
    reference: chr 1
allele count: 15
allele frequency: 1.704739174906239e-4
allele num: 87990
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+26G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+26G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+26G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+26G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+26G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+26G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+26G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+26G>A
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17594
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15073
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14525
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19033
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3606
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15516
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

1-6341137-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341137
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341137
    reference: chr 1
allele count: 5
allele frequency: 5.615832154008581e-5
allele num: 89034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+25G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+25G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+25G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+25G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+25G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+25G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+25G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+25G>A
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13427
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14754
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19295
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20849
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4337
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5751
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

1-6341138-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341138
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341138
    reference: chr 1
allele count: 2
allele frequency: 2.214103841470165e-5
allele num: 90330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+24C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+24C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+24C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+24C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+24C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+24C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+24C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+24C>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12011
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3937
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22621
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 956
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14900
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

1-6341140-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341140
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341140
    reference: chr 1
allele count: 10
allele frequency: 1.069953564015322e-4
allele num: 93462
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+22G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+22G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+22G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+22G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+22G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+22G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+22G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+22G>A
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25312
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9445
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13061
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 3964
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

1-6341141-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341141
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341141
    reference: chr 1
allele count: 3
allele frequency: 3.138928997426078e-5
allele num: 95574
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+21C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+21C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+21C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+21C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+21C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+21C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+21C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+21C>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7446
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7893
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3301
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12787
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1599
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

1-6341142-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341142
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341142
    reference: chr 1
allele count: 4
allele frequency: 4.118955432902216e-5
allele num: 97112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+20A>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+20A>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+20A>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+20A>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+20A>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+20A>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+20A>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+20A>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29164
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1224
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12118
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30383
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2893
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

1-6341144-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341144
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341144
    reference: chr 1
allele count: 111
allele frequency: 1.115331283535299e-3
allele num: 99522
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+18G>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+18G>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+18G>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+18G>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+18G>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+18G>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+18G>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+18G>C
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31448
  bin: 2.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7990
  bin: 2.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 1.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10370
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2371
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1105
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5160
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10977
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 5
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/1-6341153-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341153
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341153
    reference: chr 1
allele count: 7
allele frequency: 6.561802808451602e-5
allele num: 106678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+9G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+9G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+9G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+9G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+9G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+9G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+9G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+9G>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35523
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7217
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36139
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

1-6341153-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341153
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341153
    reference: chr 1
allele count: 1
allele frequency: 9.374004012073717e-6
allele num: 106678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+9G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+9G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+9G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+9G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+9G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+9G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+9G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+9G>A
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1322
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5740
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

1-6341154-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341154
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341154
    reference: chr 1
allele count: 539
allele frequency: 4.966277226992961e-3
allele num: 108532
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+8C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+8C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+8C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+8C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+8C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+8C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+8C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+8C>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 1.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 35746
  bin: 2.25e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 3.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10008
  bin: 2.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 9.75e1
  variant carriers: 503
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 3.75e1
  variant carriers: 3
hgvs: c.1044+8C>T
num of homozygotes: 14
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ

1-6341155-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341155
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341155
    reference: chr 1
allele count: 4
allele frequency: 3.654436485893875e-5
allele num: 109456
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1014+7G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*139+7G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.918+7G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1044+7G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*342+7G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.891+7G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.954+7G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.699+7G>A
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10121
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6104
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
hgvs: c.1044+7G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

1-6341165-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341165
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341165
    reference: chr 1
allele count: 3
allele frequency: 2.634444483473252e-5
allele num: 113876
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.951G>A
  hgvsp: ENST00000377845.3:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1041G>A
  hgvsp: ENST00000377855.2:c.1041G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1011G>A
  hgvsp: ENST00000361521.4:c.1011G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*339G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*136G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.915G>A
  hgvsp: ENST00000608083.1:c.915G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.696G>A
  hgvsp: ENST00000545482.1:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.888G>A
  hgvsp: ENST00000377842.3:c.888G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu347Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

1-6341171-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341171
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341171
    reference: chr 1
allele count: 1
allele frequency: 8.639756704451203e-6
allele num: 115744
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.909C>T
  hgvsp: ENST00000608083.1:c.909C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.882C>T
  hgvsp: ENST00000377842.3:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1005C>T
  hgvsp: ENST00000361521.4:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*333C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1035C>T
  hgvsp: ENST00000377855.2:c.1035C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.690C>T
  hgvsp: ENST00000545482.1:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.945C>T
  hgvsp: ENST00000377845.3:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*130C>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38369
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro345Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

1-6341172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341172
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341172
    reference: chr 1
allele count: 1
allele frequency: 8.624258313785014e-6
allele num: 115952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.944C>T
  hgvsp: ENSP00000367076.3:p.Pro315Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.1004C>T
  hgvsp: ENSP00000354615.4:p.Pro335Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.881C>T
  hgvsp: ENSP00000367073.3:p.Pro294Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1034C>T
  hgvsp: ENSP00000367086.2:p.Pro345Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.908C>T
  hgvsp: ENSP00000476610.1:p.Pro303Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.689C>T
  hgvsp: ENSP00000439218.1:p.Pro230Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*129C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*332C>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro345Leu
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/1-6341177-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341177
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341177
    reference: chr 1
allele count: 1
allele frequency: 8.556808652644909e-6
allele num: 116866
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*327T>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.684T>G
  hgvsp: ENST00000545482.1:c.684T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.999T>G
  hgvsp: ENST00000361521.4:c.999T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1029T>G
  hgvsp: ENST00000377855.2:c.1029T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.903T>G
  hgvsp: ENST00000608083.1:c.903T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.939T>G
  hgvsp: ENST00000377845.3:c.939T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.876T>G
  hgvsp: ENST00000377842.3:c.876T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*124T>G
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7156
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40370
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro343Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP

1-6341182-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341182
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341182
    reference: chr 1
allele count: 1
allele frequency: 8.505715841045183e-6
allele num: 117568
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*322C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*119C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.679C>T
  hgvsp: ENST00000545482.1:c.679C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.898C>T
  hgvsp: ENST00000608083.1:c.898C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1024C>T
  hgvsp: ENST00000377855.2:c.1024C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.994C>T
  hgvsp: ENST00000361521.4:c.994C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.934C>T
  hgvsp: ENST00000377845.3:c.934C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.871C>T
  hgvsp: ENST00000377842.3:c.871C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu342Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/1-6341183-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341183
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341183
    reference: chr 1
allele count: 7
allele frequency: 5.949648970710728e-5
allele num: 117654
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.933G>T
  hgvsp: ENST00000377845.3:c.933G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.678G>T
  hgvsp: ENST00000545482.1:c.678G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.993G>T
  hgvsp: ENST00000361521.4:c.993G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*321G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*118G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1023G>T
  hgvsp: ENST00000377855.2:c.1023G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.897G>T
  hgvsp: ENST00000608083.1:c.897G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.870G>T
  hgvsp: ENST00000377842.3:c.870G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2370
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1769
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser341Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

1-6341183-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341183
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341183
    reference: chr 1
allele count: 8
allele frequency: 6.799598823669403e-5
allele num: 117654
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*321G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.993G>A
  hgvsp: ENST00000361521.4:c.993G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1023G>A
  hgvsp: ENST00000377855.2:c.1023G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.870G>A
  hgvsp: ENST00000377842.3:c.870G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.678G>A
  hgvsp: ENST00000545482.1:c.678G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*118G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.897G>A
  hgvsp: ENST00000608083.1:c.897G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.933G>A
  hgvsp: ENST00000377845.3:c.933G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser341Ser
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

1-6341186-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341186
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341186
    reference: chr 1
allele count: 11
allele frequency: 9.29917998140164e-5
allele num: 118290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.990G>A
  hgvsp: ENST00000361521.4:c.990G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.867G>A
  hgvsp: ENST00000377842.3:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.930G>A
  hgvsp: ENST00000377845.3:c.930G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.894G>A
  hgvsp: ENST00000608083.1:c.894G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1020G>A
  hgvsp: ENST00000377855.2:c.1020G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.675G>A
  hgvsp: ENST00000545482.1:c.675G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*318G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*115G>A
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38420
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2432
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg340Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

1-6341188-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341188
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341188
    reference: chr 1
allele count: 2
allele frequency: 1.686909581646424e-5
allele num: 118560
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.988A>T
  hgvsp: ENSP00000354615.4:p.Arg330Trp
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*113A>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.928A>T
  hgvsp: ENSP00000367076.3:p.Arg310Trp
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.673A>T
  hgvsp: ENSP00000439218.1:p.Arg225Trp
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.892A>T
  hgvsp: ENSP00000476610.1:p.Arg298Trp
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1018A>T
  hgvsp: ENSP00000367086.2:p.Arg340Trp
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.865A>T
  hgvsp: ENSP00000367073.3:p.Arg289Trp
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*316A>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40969
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7506
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg340Trp
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

1-6341192-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341192
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341192
    reference: chr 1
allele count: 1
allele frequency: 8.402655239055541e-6
allele num: 119010
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.888A>G
  hgvsp: ENST00000608083.1:c.888A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.837A>G
  hgvsp: ENST00000473466.1:c.837A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.924A>G
  hgvsp: ENST00000377845.3:c.924A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.984A>G
  hgvsp: ENST00000361521.4:c.984A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.861A>G
  hgvsp: ENST00000377842.3:c.861A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*109A>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.669A>G
  hgvsp: ENST00000545482.1:c.669A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1014A>G
  hgvsp: ENST00000377855.2:c.1014A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*312A>G
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7585
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu338Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD

1-6341199-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341199
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341199
    reference: chr 1
allele count: 1
allele frequency: 8.36638053645232e-6
allele num: 119526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.854G>A
  hgvsp: ENSP00000367073.3:p.Ser285Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.830G>A
  hgvsp: ENSP00000465719.1:p.Ser277Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*102G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*305G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.881G>A
  hgvsp: ENSP00000476610.1:p.Ser294Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.977G>A
  hgvsp: ENSP00000354615.4:p.Ser326Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.917G>A
  hgvsp: ENSP00000367076.3:p.Ser306Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.662G>A
  hgvsp: ENSP00000439218.1:p.Ser221Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1007G>A
  hgvsp: ENSP00000367086.2:p.Ser336Asn
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser336Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

1-6341205-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341205
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341205
    reference: chr 1
allele count: 2
allele frequency: 1.668335001668335e-5
allele num: 119880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.911C>T
  hgvsp: ENSP00000367076.3:p.Ser304Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.875C>T
  hgvsp: ENSP00000476610.1:p.Ser292Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.1001C>T
  hgvsp: ENSP00000367086.2:p.Ser334Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.824C>T
  hgvsp: ENSP00000465719.1:p.Ser275Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*96C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.848C>T
  hgvsp: ENSP00000367073.3:p.Ser283Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.971C>T
  hgvsp: ENSP00000354615.4:p.Ser324Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*299C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.656C>T
  hgvsp: ENSP00000439218.1:p.Ser219Leu
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41306
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2554
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser334Leu
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-6341209-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341209
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341209
    reference: chr 1
allele count: 1
allele frequency: 8.329030001166064e-6
allele num: 120062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.844G>T
  hgvsp: ENSP00000367073.3:p.Val282Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*92G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.997G>T
  hgvsp: ENSP00000367086.2:p.Val333Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.820G>T
  hgvsp: ENSP00000465719.1:p.Val274Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.871G>T
  hgvsp: ENSP00000476610.1:p.Val291Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.652G>T
  hgvsp: ENSP00000439218.1:p.Val218Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*295G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.967G>T
  hgvsp: ENSP00000354615.4:p.Val323Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.907G>T
  hgvsp: ENSP00000367076.3:p.Val303Leu
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2974
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val333Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

1-6341216-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341216
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341216
    reference: chr 1
allele count: 3
allele frequency: 2.493185293531015e-5
allele num: 120328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.813C>T
  hgvsp: ENST00000473466.1:c.813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.645C>T
  hgvsp: ENST00000545482.1:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.837C>T
  hgvsp: ENST00000377842.3:c.837C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.960C>T
  hgvsp: ENST00000361521.4:c.960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*85C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*288C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.900C>T
  hgvsp: ENST00000377845.3:c.900C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.990C>T
  hgvsp: ENST00000377855.2:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.864C>T
  hgvsp: ENST00000608083.1:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7839
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe330Phe
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

1-6341234-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341234
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341234
    reference: chr 1
allele count: 1
allele frequency: 8.290086714307032e-6
allele num: 120626
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.972G>A
  hgvsp: ENST00000377855.2:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*67G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.942G>A
  hgvsp: ENST00000361521.4:c.942G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.819G>A
  hgvsp: ENST00000377842.3:c.819G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.846G>A
  hgvsp: ENST00000608083.1:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.882G>A
  hgvsp: ENST00000377845.3:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.627G>A
  hgvsp: ENST00000545482.1:c.627G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.795G>A
  hgvsp: ENST00000473466.1:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*270G>A
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6332
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3032
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg324Arg
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

1-6341238-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341238
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341238
    reference: chr 1
allele count: 1
allele frequency: 8.287613333112331e-6
allele num: 120662
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.815A>G
  hgvsp: ENSP00000367073.3:p.Tyr272Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.878A>G
  hgvsp: ENSP00000367076.3:p.Tyr293Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*266A>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.968A>G
  hgvsp: ENSP00000367086.2:p.Tyr323Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.791A>G
  hgvsp: ENSP00000465719.1:p.Tyr264Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.938A>G
  hgvsp: ENSP00000354615.4:p.Tyr313Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*63A>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.623A>G
  hgvsp: ENSP00000439218.1:p.Tyr208Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.842A>G
  hgvsp: ENSP00000476610.1:p.Tyr281Cys
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2633
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr323Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

1-6341241-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341241
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341241
    reference: chr 1
allele count: 1
allele frequency: 8.279242283746192e-6
allele num: 120784
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.875G>A
  hgvsp: ENSP00000367076.3:p.Arg292His
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.620G>A
  hgvsp: ENSP00000439218.1:p.Arg207His
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.788G>A
  hgvsp: ENSP00000465719.1:p.Arg263His
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*60G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.812G>A
  hgvsp: ENSP00000367073.3:p.Arg271His
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.935G>A
  hgvsp: ENSP00000354615.4:p.Arg312His
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.965G>A
  hgvsp: ENSP00000367086.2:p.Arg322His
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.839G>A
  hgvsp: ENSP00000476610.1:p.Arg280His
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*263G>A
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2642
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1983
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg322His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

1-6341242-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341242
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341242
    reference: chr 1
allele count: 10
allele frequency: 8.278145695364238e-5
allele num: 120800
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.964C>T
  hgvsp: ENSP00000367086.2:p.Arg322Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.811C>T
  hgvsp: ENSP00000367073.3:p.Arg271Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.787C>T
  hgvsp: ENSP00000465719.1:p.Arg263Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*262C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.619C>T
  hgvsp: ENSP00000439218.1:p.Arg207Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.934C>T
  hgvsp: ENSP00000354615.4:p.Arg312Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.838C>T
  hgvsp: ENSP00000476610.1:p.Arg280Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*59C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.874C>T
  hgvsp: ENSP00000367076.3:p.Arg292Cys
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1982
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg322Cys
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD

1-6341253-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341253
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341253
    reference: chr 1
allele count: 1
allele frequency: 8.268152729317216e-6
allele num: 120946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.776G>A
  hgvsp: ENSP00000465719.1:p.Ser259Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*48G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.827G>A
  hgvsp: ENSP00000476610.1:p.Ser276Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*251G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.800G>A
  hgvsp: ENSP00000367073.3:p.Ser267Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.608G>A
  hgvsp: ENSP00000439218.1:p.Ser203Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.923G>A
  hgvsp: ENSP00000354615.4:p.Ser308Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.953G>A
  hgvsp: ENSP00000367086.2:p.Ser318Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.863G>A
  hgvsp: ENSP00000367076.3:p.Ser288Asn
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1984
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser318Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/1-6341261-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341261
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341261
    reference: chr 1
allele count: 1
allele frequency: 8.263643275047103e-6
allele num: 121012
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.855T>G
  hgvsp: ENST00000377845.3:c.855T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*243T>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.819T>G
  hgvsp: ENST00000608083.1:c.819T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.792T>G
  hgvsp: ENST00000377842.3:c.792T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.915T>G
  hgvsp: ENST00000361521.4:c.915T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*40T>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.945T>G
  hgvsp: ENST00000377855.2:c.945T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.600T>G
  hgvsp: ENST00000545482.1:c.600T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.768T>G
  hgvsp: ENST00000473466.1:c.768T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2652
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val315Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

1-6341267-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341267
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341267
    reference: chr 1
allele count: 2
allele frequency: 1.651855033202286e-5
allele num: 121076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.813C>A
  hgvsp: ENSP00000476610.1:p.Asp271Glu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.594C>A
  hgvsp: ENSP00000439218.1:p.Asp198Glu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.762C>A
  hgvsp: ENSP00000465719.1:p.Asp254Glu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*237C>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.909C>A
  hgvsp: ENSP00000354615.4:p.Asp303Glu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.849C>A
  hgvsp: ENSP00000367076.3:p.Asp283Glu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.786C>A
  hgvsp: ENSP00000367073.3:p.Asp262Glu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*34C>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.939C>A
  hgvsp: ENSP00000367086.2:p.Asp313Glu
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp313Glu
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

1-6341269-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341269
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341269
    reference: chr 1
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.760G>A
  hgvsp: ENSP00000465719.1:p.Asp254Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.592G>A
  hgvsp: ENSP00000439218.1:p.Asp198Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*32G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.784G>A
  hgvsp: ENSP00000367073.3:p.Asp262Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.811G>A
  hgvsp: ENSP00000476610.1:p.Asp271Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.937G>A
  hgvsp: ENSP00000367086.2:p.Asp313Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.847G>A
  hgvsp: ENSP00000367076.3:p.Asp283Asn
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*235G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.907G>A
  hgvsp: ENSP00000354615.4:p.Asp303Asn
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1988
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp313Asn
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

1-6341270-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341270
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341270
    reference: chr 1
allele count: 3
allele frequency: 2.477987213585978e-5
allele num: 121066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.810C>T
  hgvsp: ENST00000608083.1:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.936C>T
  hgvsp: ENST00000377855.2:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.846C>T
  hgvsp: ENST00000377845.3:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.783C>T
  hgvsp: ENST00000377842.3:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.759C>T
  hgvsp: ENST00000473466.1:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.591C>T
  hgvsp: ENST00000545482.1:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*234C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*31C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.906C>T
  hgvsp: ENST00000361521.4:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala312Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

1-6341272-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341272
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341272
    reference: chr 1
allele count: 1
allele frequency: 8.258593066085262e-6
allele num: 121086
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.934G>A
  hgvsp: ENSP00000367086.2:p.Ala312Thr
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.757G>A
  hgvsp: ENSP00000465719.1:p.Ala253Thr
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*29G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*232G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.589G>A
  hgvsp: ENSP00000439218.1:p.Ala197Thr
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.904G>A
  hgvsp: ENSP00000354615.4:p.Ala302Thr
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.781G>A
  hgvsp: ENSP00000367073.3:p.Ala261Thr
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.844G>A
  hgvsp: ENSP00000367076.3:p.Ala282Thr
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.808G>A
  hgvsp: ENSP00000476610.1:p.Ala270Thr
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7971
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3061
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala312Thr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

1-6341273-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341273
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341273
    reference: chr 1
allele count: 10
allele frequency: 8.258047467256842e-5
allele num: 121094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.588C>T
  hgvsp: ENST00000545482.1:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.933C>T
  hgvsp: ENST00000377855.2:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.807C>T
  hgvsp: ENST00000608083.1:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.903C>T
  hgvsp: ENST00000361521.4:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.756C>T
  hgvsp: ENST00000473466.1:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.780C>T
  hgvsp: ENST00000377842.3:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.843C>T
  hgvsp: ENST00000377845.3:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*231C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*28C>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7970
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42249
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp311Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

1-6341276-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341276
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341276
    reference: chr 1
allele count: 1
allele frequency: 8.257638315441784e-6
allele num: 121100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.777G>A
  hgvsp: ENST00000377842.3:c.777G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.804G>A
  hgvsp: ENST00000608083.1:c.804G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.900G>A
  hgvsp: ENST00000361521.4:c.900G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.585G>A
  hgvsp: ENST00000545482.1:c.585G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.930G>A
  hgvsp: ENST00000377855.2:c.930G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.753G>A
  hgvsp: ENST00000473466.1:c.753G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.840G>A
  hgvsp: ENST00000377845.3:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*228G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*25G>A
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2650
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val310Val
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS

1-6341279-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341279
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341279
    reference: chr 1
allele count: 3
allele frequency: 2.476882430647292e-5
allele num: 121120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.582G>A
  hgvsp: ENST00000545482.1:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*22G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.927G>A
  hgvsp: ENST00000377855.2:c.927G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.750G>A
  hgvsp: ENST00000473466.1:c.750G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.774G>A
  hgvsp: ENST00000377842.3:c.774G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*225G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.837G>A
  hgvsp: ENST00000377845.3:c.837G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.897G>A
  hgvsp: ENST00000361521.4:c.897G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.801G>A
  hgvsp: ENST00000608083.1:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu309Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

1-6341281-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341281
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341281
    reference: chr 1
allele count: 1
allele frequency: 8.255865792645674e-6
allele num: 121126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*223T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.748T>C
  hgvsp: ENST00000473466.1:c.748T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*20T>C
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.895T>C
  hgvsp: ENST00000361521.4:c.895T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.925T>C
  hgvsp: ENST00000377855.2:c.925T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.799T>C
  hgvsp: ENST00000608083.1:c.799T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.835T>C
  hgvsp: ENST00000377845.3:c.835T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.580T>C
  hgvsp: ENST00000545482.1:c.580T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.772T>C
  hgvsp: ENST00000377842.3:c.772T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3065
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu309Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/1-6341284-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341284
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341284
    reference: chr 1
allele count: 1
allele frequency: 8.255184255712587e-6
allele num: 121136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*17G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.796G>T
  hgvsp: ENSP00000476610.1:p.Val266Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*220G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.922G>T
  hgvsp: ENSP00000367086.2:p.Val308Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.769G>T
  hgvsp: ENSP00000367073.3:p.Val257Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.892G>T
  hgvsp: ENSP00000354615.4:p.Val298Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.832G>T
  hgvsp: ENSP00000367076.3:p.Val278Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.577G>T
  hgvsp: ENSP00000439218.1:p.Val193Leu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.745G>T
  hgvsp: ENSP00000465719.1:p.Val249Leu
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val308Leu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

1-6341288-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341288
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341288
    reference: chr 1
allele count: 5
allele frequency: 4.127115146512587e-5
allele num: 121150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.888C>T
  hgvsp: ENST00000361521.4:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.828C>T
  hgvsp: ENST00000377845.3:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*13C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.792C>T
  hgvsp: ENST00000608083.1:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.741C>T
  hgvsp: ENST00000473466.1:c.741C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.918C>T
  hgvsp: ENST00000377855.2:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.573C>T
  hgvsp: ENST00000545482.1:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.765C>T
  hgvsp: ENST00000377842.3:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*216C>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14415
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6393
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3064
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42291
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile306Ile
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

1-6341299-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341299
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341299
    reference: chr 1
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.754T>A
  hgvsp: ENSP00000367073.3:p.Ser252Thr
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.817T>A
  hgvsp: ENSP00000367076.3:p.Ser273Thr
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*205T>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.877T>A
  hgvsp: ENSP00000354615.4:p.Ser293Thr
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.730T>A
  hgvsp: ENSP00000465719.1:p.Ser244Thr
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.562T>A
  hgvsp: ENSP00000439218.1:p.Ser188Thr
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.781T>A
  hgvsp: ENSP00000476610.1:p.Ser261Thr
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.*2T>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.907T>A
  hgvsp: ENSP00000367086.2:p.Ser303Thr
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 960
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42323
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser303Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

1-6341304-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341304
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341304
    reference: chr 1
allele count: 4
allele frequency: 3.301474108189306e-5
allele num: 121158
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.557A>G
  hgvsp: ENSP00000439218.1:p.Asn186Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.812A>G
  hgvsp: ENSP00000367076.3:p.Asn271Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.749A>G
  hgvsp: ENSP00000367073.3:p.Asn250Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.902A>G
  hgvsp: ENSP00000367086.2:p.Asn301Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.849A>G
  hgvsp: ENST00000377860.4:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.725A>G
  hgvsp: ENSP00000465719.1:p.Asn242Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.776A>G
  hgvsp: ENSP00000476610.1:p.Asn259Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*200A>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.872A>G
  hgvsp: ENSP00000354615.4:p.Asn291Ser
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn301Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS

1-6341309-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341309
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341309
    reference: chr 1
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.844G>C
  hgvsp: ENSP00000367091.4:p.Glu282Gln
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.744G>C
  hgvsp: ENST00000377842.3:c.744G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.720G>C
  hgvsp: ENST00000473466.1:c.720G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.552G>C
  hgvsp: ENST00000545482.1:c.552G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.897G>C
  hgvsp: ENST00000377855.2:c.897G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.771G>C
  hgvsp: ENST00000608083.1:c.771G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.867G>C
  hgvsp: ENST00000361521.4:c.867G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.807G>C
  hgvsp: ENST00000377845.3:c.807G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*195G>C
  variant of: http://identifiers.org/hgnc/24157
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu282Gln
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

1-6341309-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341309
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341309
    reference: chr 1
allele count: 113
allele frequency: 9.327742191111405e-4
allele num: 121144
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.720G>A
  hgvsp: ENST00000473466.1:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.844G>A
  hgvsp: ENSP00000367091.4:p.Glu282Lys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.771G>A
  hgvsp: ENST00000608083.1:c.771G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.867G>A
  hgvsp: ENST00000361521.4:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.807G>A
  hgvsp: ENST00000377845.3:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.552G>A
  hgvsp: ENST00000545482.1:c.552G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.744G>A
  hgvsp: ENST00000377842.3:c.744G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*195G>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.897G>A
  hgvsp: ENST00000377855.2:c.897G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 37776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14394
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42246
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu282Lys
num of homozygotes: 1
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

1-6341311-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341311
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341311
    reference: chr 1
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*193A>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.895A>G
  hgvsp: ENSP00000367086.2:p.Thr299Ala
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.550A>G
  hgvsp: ENSP00000439218.1:p.Thr184Ala
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.865A>G
  hgvsp: ENSP00000354615.4:p.Thr289Ala
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.842A>G
  hgvsp: ENSP00000367091.4:p.His281Arg
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.769A>G
  hgvsp: ENSP00000476610.1:p.Thr257Ala
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.742A>G
  hgvsp: ENSP00000367073.3:p.Thr248Ala
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.718A>G
  hgvsp: ENSP00000465719.1:p.Thr240Ala
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.805A>G
  hgvsp: ENSP00000367076.3:p.Thr269Ala
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr299Ala
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-6341316-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341316
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341316
    reference: chr 1
allele count: 1
allele frequency: 8.255865792645674e-6
allele num: 121126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.800C>G
  hgvsp: ENSP00000367076.3:p.Thr267Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.545C>G
  hgvsp: ENSP00000439218.1:p.Thr182Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.837C>G
  hgvsp: ENSP00000367091.4:p.Asp279Glu
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.890C>G
  hgvsp: ENSP00000367086.2:p.Thr297Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000097021
  ensembl transcript: ENST00000481175
  gene symbol: ACOT7
  hgvsc: ENST00000481175.1:n.745C>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.764C>G
  hgvsp: ENSP00000476610.1:p.Thr255Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.860C>G
  hgvsp: ENSP00000354615.4:p.Thr287Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.713C>G
  hgvsp: ENSP00000465719.1:p.Thr238Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*188C>G
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.737C>G
  hgvsp: ENSP00000367073.3:p.Thr246Ser
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr297Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

1-6341321-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341321
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341321
    reference: chr 1
allele count: 1
allele frequency: 8.258593066085262e-6
allele num: 121086
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.855C>T
  hgvsp: ENST00000361521.4:c.855C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000097021
  ensembl transcript: ENST00000481175
  gene symbol: ACOT7
  hgvsc: ENST00000481175.1:n.740C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.832C>T
  hgvsp: ENSP00000367091.4:p.His278Tyr
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.885C>T
  hgvsp: ENST00000377855.2:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.795C>T
  hgvsp: ENST00000377845.3:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.732C>T
  hgvsp: ENST00000377842.3:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.759C>T
  hgvsp: ENST00000608083.1:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*183C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.708C>T
  hgvsp: ENST00000473466.1:c.708C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.540C>T
  hgvsp: ENST00000545482.1:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His278Tyr
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

1-6341323-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341323
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341323
    reference: chr 1
allele count: 2
allele frequency: 1.652018766933192e-5
allele num: 121064
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*181C>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.883C>T
  hgvsp: ENSP00000367086.2:p.Arg295Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.730C>T
  hgvsp: ENSP00000367073.3:p.Arg244Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.538C>T
  hgvsp: ENSP00000439218.1:p.Arg180Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.793C>T
  hgvsp: ENSP00000367076.3:p.Arg265Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.853C>T
  hgvsp: ENSP00000354615.4:p.Arg285Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.706C>T
  hgvsp: ENSP00000465719.1:p.Arg236Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.757C>T
  hgvsp: ENSP00000476610.1:p.Arg253Cys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.830C>T
  hgvsp: ENSP00000367091.4:p.Thr277Met
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000097021
  ensembl transcript: ENST00000481175
  gene symbol: ACOT7
  hgvsc: ENST00000481175.1:n.738C>T
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7931
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg295Cys
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

1-6341323-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341323
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341323
    reference: chr 1
allele count: 1
allele frequency: 8.260093834665961e-6
allele num: 121064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.830C>A
  hgvsp: ENSP00000367091.4:p.Thr277Lys
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.730C>A
  hgvsp: ENSP00000367073.3:p.Arg244Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.793C>A
  hgvsp: ENSP00000367076.3:p.Arg265Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000097021
  ensembl transcript: ENST00000481175
  gene symbol: ACOT7
  hgvsc: ENST00000481175.1:n.738C>A
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.757C>A
  hgvsp: ENSP00000476610.1:p.Arg253Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.883C>A
  hgvsp: ENSP00000367086.2:p.Arg295Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.853C>A
  hgvsp: ENSP00000354615.4:p.Arg285Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.706C>A
  hgvsp: ENSP00000465719.1:p.Arg236Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.538C>A
  hgvsp: ENSP00000439218.1:p.Arg180Ser
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*181C>A
  variant of: http://identifiers.org/hgnc/24157
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg295Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/1-6341327-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6341327
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 6341327
    reference: chr 1
allele count: 1
allele frequency: 8.261595148791329e-6
allele num: 121042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000476610
  ensembl transcript: ENST00000608083
  gene symbol: ACOT7
  hgvsc: ENST00000608083.1:c.753G>T
  hgvsp: ENST00000608083.1:c.753G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000402532
  ensembl transcript: ENST00000418124
  gene symbol: ACOT7
  hgvsc: ENST00000418124.1:c.*177G>T
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367076
  ensembl transcript: ENST00000377845
  gene symbol: ACOT7
  hgvsc: ENST00000377845.3:c.789G>T
  hgvsp: ENST00000377845.3:c.789G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000354615
  ensembl transcript: ENST00000361521
  gene symbol: ACOT7
  hgvsc: ENST00000361521.4:c.849G>T
  hgvsp: ENST00000361521.4:c.849G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367073
  ensembl transcript: ENST00000377842
  gene symbol: ACOT7
  hgvsc: ENST00000377842.3:c.726G>T
  hgvsp: ENST00000377842.3:c.726G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000439218
  ensembl transcript: ENST00000545482
  gene symbol: ACOT7
  hgvsc: ENST00000545482.1:c.534G>T
  hgvsp: ENST00000545482.1:c.534G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000465719
  ensembl transcript: ENST00000473466
  gene symbol: ACOT7
  hgvsc: ENST00000473466.1:c.702G>T
  hgvsp: ENST00000473466.1:c.702G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367091
  ensembl transcript: ENST00000377860
  gene symbol: ACOT7
  hgvsc: ENST00000377860.4:c.826G>T
  hgvsp: ENSP00000367091.4:p.Gly276Trp
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000097021
  ensembl protein: ENSP00000367086
  ensembl transcript: ENST00000377855
  gene symbol: ACOT7
  hgvsc: ENST00000377855.2:c.879G>T
  hgvsp: ENST00000377855.2:c.879G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24157
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000097021
  ensembl transcript: ENST00000481175
  gene symbol: ACOT7
  hgvsc: ENST00000481175.1:n.734G>T
  variant of: http://identifiers.org/hgnc/24157
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2636
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly276Trp
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

GenotypeQuality
all individuals: 349
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 184
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4157
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10004
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5996
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64482
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.264879087833605e-5
allele num: 15962
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.793e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.51534e6

VQSLOD
type: SiteQuality
SIO_000300: 6.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: 1.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.007e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 320
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4032
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46239
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.554581351242111e-4
allele num: 64326
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.653927813163482e-4
allele num: 11304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15902
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.176193836744295e-4
allele num: 8502
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.018054162487463e-4
allele num: 9970
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.117e1

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

DP
type: SiteQuality
SIO_000300: 1.509906e6

VQSLOD
type: SiteQuality
SIO_000300: 3.93e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.45e-1

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

GenotypeQuality
all individuals: 218
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 707
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 241
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 633
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 748
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 476
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3695
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 43703
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3706
bin: 9.75e1
variant carriers: 1403

GenotypeQuality
all individuals: 362
bin: 7.5e0
variant carriers: 1

Other
type: Population
allele count: 24
allele frequency: 2.816901408450704e-2
allele num: 852
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.187648456057007e-4
allele num: 8420
num of homozygotes: 0

South Asian
type: Population
allele count: 63
allele frequency: 4.00355871886121e-3
allele num: 15736
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 72
allele frequency: 1.219925449000339e-2
allele num: 5902
num of homozygotes: 0

African
type: Population
allele count: 605
allele frequency: 6.106176826806621e-2
allele num: 9908
num of homozygotes: 14

Latino
type: Population
allele count: 149
allele frequency: 1.322798295454545e-2
allele num: 11264
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 532
allele frequency: 8.330201678566955e-3
allele num: 63864
num of homozygotes: 3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.81e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 5.639999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.34e0

DP
type: SiteQuality
SIO_000300: 1.5178e6

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

QD
type: SiteQuality
SIO_000300: 1.354e1

GenotypeQuality
all individuals: 425
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4852
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2434
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 43088
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3708
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11208
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.576839383140433e-5
allele num: 63418
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15578
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5838
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.11e0

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.474126e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQ
type: SiteQuality
SIO_000300: 6.012e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.14e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

GenotypeQuality
all individuals: 5021
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42867
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2441
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 390
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1036
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3657
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63330
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.596928982725527e-4
allele num: 8336
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: 11186
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15566
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.286e0

DP
type: SiteQuality
SIO_000300: 1.470654e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e-1

QD
type: SiteQuality
SIO_000300: 1.143e1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5021
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3657
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2441
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 544
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11186
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.199616122840691e-4
allele num: 8336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63330
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15566
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.51e-1

QD
type: SiteQuality
SIO_000300: 1.143e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 1.286e0

DP
type: SiteQuality
SIO_000300: 1.470654e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

GenotypeQuality
all individuals: 1171
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42410
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2433
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3632
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.187648456057007e-3
allele num: 842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63146
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5798
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.94e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

QD
type: SiteQuality
SIO_000300: 1.357e1

DP
type: SiteQuality
SIO_000300: 1.461181e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.245e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 5.75e1
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GenotypeQuality
all individuals: 1359
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15084
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.243383497664764e-5
allele num: 61664
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8042
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

DP
type: SiteQuality
SIO_000300: 1.367988e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e0

MQRankSum
type: SiteQuality
SIO_000300: 6.27e-1

FS
type: SiteQuality
SIO_000300: 5.001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.341e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

QD
type: SiteQuality
SIO_000300: 1.501e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

GenotypeQuality
all individuals: 112
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2425
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 19

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.782779505647405e-4
allele num: 61090
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7932
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10688
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.339584728734092e-4
allele num: 14930
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.599e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

DP
type: SiteQuality
SIO_000300: 1.321918e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

FS
type: SiteQuality
SIO_000300: 1.438e0

VQSLOD
type: SiteQuality
SIO_000300: 3.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.24e-1

GenotypeQuality
all individuals: 75
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11464
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variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2432
bin: 9.75e1
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
all individuals: 126
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variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.638860664066341e-5
allele num: 61018
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7924
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10704
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14942
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

FS
type: SiteQuality
SIO_000300: 1.89e0

VQSLOD
type: SiteQuality
SIO_000300: -1.456e-1

DP
type: SiteQuality
SIO_000300: 1.32011e6

MQRankSum
type: SiteQuality
SIO_000300: -6.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.395e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.822e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.15e-1

GenotypeQuality
all individuals: 348
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14229
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variant carriers: 0

GenotypeQuality
all individuals: 4842
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 217
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GenotypeQuality
all individuals: 1735
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1062
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GenotypeQuality
all individuals: 2430
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20710
bin: 6.25e1
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GenotypeQuality
all individuals: 455
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7740
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59980
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14690
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.083658430862592e-4
allele num: 9228
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5410
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.809e1

MQRankSum
type: SiteQuality
SIO_000300: -1.247e0

DP
type: SiteQuality
SIO_000300: 1.204469e6

FS
type: SiteQuality
SIO_000300: 9.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.779e0

QD
type: SiteQuality
SIO_000300: 1.634e1

VQSLOD
type: SiteQuality
SIO_000300: -4.582e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.42e0

GenotypeQuality
all individuals: 1137
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7172
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variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 7.5e0
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GenotypeQuality
all individuals: 919
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variant carriers: 0

GenotypeQuality
all individuals: 1712
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14384
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variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 318
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GenotypeQuality
all individuals: 19725
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GenotypeQuality
all individuals: 282
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.523809523809524e-5
allele num: 10500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5372
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14650
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7720
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9196
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.903e0

DP
type: SiteQuality
SIO_000300: 1.192624e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.174e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.71e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.4e-2

GenotypeQuality
all individuals: 2785
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2447
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 217
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GenotypeQuality
all individuals: 418
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GenotypeQuality
all individuals: 270
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GenotypeQuality
all individuals: 5817
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variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 7.5e0
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GenotypeQuality
all individuals: 162
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variant carriers: 0

GenotypeQuality
all individuals: 277
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variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 19
allele frequency: 1.904570970328789e-3
allele num: 9976
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14024
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8776
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57514
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

DP
type: SiteQuality
SIO_000300: 1.090403e6

QD
type: SiteQuality
SIO_000300: 1.243e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.843e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

FS
type: SiteQuality
SIO_000300: 2.688e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

GenotypeQuality
all individuals: 4306
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
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variant carriers: 0

GenotypeQuality
all individuals: 1320
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GenotypeQuality
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GenotypeQuality
all individuals: 5849
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 231
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 4842
bin: 6.25e1
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GenotypeQuality
all individuals: 422
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variant carriers: 2

GenotypeQuality
all individuals: 164
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GenotypeQuality
all individuals: 12406
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 26
allele frequency: 1.888711317739358e-3
allele num: 13766
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6998
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.053809817210926e-4
allele num: 9738
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4868
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.336898395721925e-3
allele num: 748
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.771479185119575e-5
allele num: 56450
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.9e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

QD
type: SiteQuality
SIO_000300: 1.36e1

DP
type: SiteQuality
SIO_000300: 1.079909e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 5548
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6431
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 583
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GenotypeQuality
all individuals: 1727
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variant carriers: 0

GenotypeQuality
all individuals: 920
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variant carriers: 0

GenotypeQuality
all individuals: 5588
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3580
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variant carriers: 0

GenotypeQuality
all individuals: 5615
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GenotypeQuality
all individuals: 416
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variant carriers: 1

GenotypeQuality
all individuals: 104
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GenotypeQuality
all individuals: 97
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3176
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13132
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.220643098241251e-5
allele num: 45032
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.106e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.8e-1

DP
type: SiteQuality
SIO_000300: 8.29744e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 1068
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14469
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
all individuals: 2351
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 9.75e1
variant carriers: 5

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13208
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5500
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 8.788890841975742e-5
allele num: 45512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3182
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6688
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.46394e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.94e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.378e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

GenotypeQuality
all individuals: 228
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 16877
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variant carriers: 0

GenotypeQuality
all individuals: 4130
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7952
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.088380252276334e-5
allele num: 47884
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

DP
type: SiteQuality
SIO_000300: 9.50586e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.825e0

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.13e-1

QD
type: SiteQuality
SIO_000300: 1.299e1

MQ
type: SiteQuality
SIO_000300: 5.923e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.22e-1

GenotypeQuality
all individuals: 221
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 9.75e1
variant carriers: 14

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.239720649613621e-4
allele num: 48398
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7094
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6008
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 1.723147616312464e-3
allele num: 3482
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13558
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

QD
type: SiteQuality
SIO_000300: 2.029e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

FS
type: SiteQuality
SIO_000300: 4.048e0

DP
type: SiteQuality
SIO_000300: 9.69796e5

GenotypeQuality
all individuals: 1103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3606
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 641
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variant carriers: 0

GenotypeQuality
all individuals: 19033
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.225490196078431e-4
allele num: 8160
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7158
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6064
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.048676554945505e-5
allele num: 48812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3544
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.85037e5

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

FS
type: SiteQuality
SIO_000300: 8.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

QD
type: SiteQuality
SIO_000300: 1.008e1

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-2

GenotypeQuality
all individuals: 553
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6256
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
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GenotypeQuality
all individuals: 3040
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variant carriers: 0

GenotypeQuality
all individuals: 4577
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variant carriers: 0

GenotypeQuality
all individuals: 460
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variant carriers: 1

GenotypeQuality
all individuals: 1030
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 156
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7158
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6064
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 3.073014832418258e-4
allele num: 48812
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8160
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13602
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.85037e5

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.52e0

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

QD
type: SiteQuality
SIO_000300: 1.008e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

FS
type: SiteQuality
SIO_000300: 8.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 159
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 15342
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 965
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variant carriers: 0

GenotypeQuality
all individuals: 393
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GenotypeQuality
all individuals: 905
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 894
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variant carriers: 0

GenotypeQuality
all individuals: 3302
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3226
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3640
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.312079555425563e-5
allele num: 13676
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.023963730569948e-5
allele num: 49408
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7226
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.893964110929853e-4
allele num: 6130
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.319e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.424e1

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.77e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.478e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.547e0

DP
type: SiteQuality
SIO_000300: 1.007528e6

GenotypeQuality
all individuals: 342
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
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variant carriers: 1

GenotypeQuality
all individuals: 314
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 2751
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 527
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GenotypeQuality
all individuals: 3685
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variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3710
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13784
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.718129926610492e-4
allele num: 7358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6250
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.620000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.037354e6

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

QD
type: SiteQuality
SIO_000300: 1.764e1

GenotypeQuality
all individuals: 3207
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13800
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GenotypeQuality
all individuals: 605
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variant carriers: 0

GenotypeQuality
all individuals: 607
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GenotypeQuality
all individuals: 4290
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GenotypeQuality
all individuals: 628
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GenotypeQuality
all individuals: 210
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GenotypeQuality
all individuals: 26736
bin: 6.25e1
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GenotypeQuality
all individuals: 1092
bin: 7.75e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 1983
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 7.913479293062516e-4
allele num: 7582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.848818412747287e-5
allele num: 51964
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.270663033605813e-4
allele num: 8808
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

DP
type: SiteQuality
SIO_000300: 1.092386e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.261e1

FS
type: SiteQuality
SIO_000300: 1.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e-1

MQ
type: SiteQuality
SIO_000300: 5.865e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
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variant carriers: 3

GenotypeQuality
all individuals: 229
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GenotypeQuality
all individuals: 29057
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variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 8.25e1
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GenotypeQuality
all individuals: 4704
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GenotypeQuality
all individuals: 1161
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GenotypeQuality
all individuals: 2772
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1165
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6750
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.289324394017535e-4
allele num: 7756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.881679963871745e-5
allele num: 53144
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 7.057163020465773e-5
allele num: 14170
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

QD
type: SiteQuality
SIO_000300: 9.619999999999999e0

DP
type: SiteQuality
SIO_000300: 1.128079e6

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

GenotypeQuality
all individuals: 1223
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1379
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2504
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4914
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6906
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14294
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 5.068423720223011e-4
allele num: 7892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4102
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53958
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.14745e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

VQSLOD
type: SiteQuality
SIO_000300: -4.799e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.203e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.38e-1

QD
type: SiteQuality
SIO_000300: 8.68e0

GenotypeQuality
all individuals: 126
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 122
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1287
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 725
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 32477
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 9.75e1
variant carriers: 101

GenotypeQuality
all individuals: 2080
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 256
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 7.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 1.235788433020267e-4
allele num: 8092
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.809299800977022e-5
allele num: 55270
num of homozygotes: 0

East Asian
type: Population
allele count: 108
allele frequency: 1.507958670762357e-2
allele num: 7162
num of homozygotes: 5

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.905123601712471e-5
allele num: 14482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4248
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.06e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

FS
type: SiteQuality
SIO_000300: 2.809e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.14e-1

QD
type: SiteQuality
SIO_000300: 1.462e1

DP
type: SiteQuality
SIO_000300: 1.182202e6

GenotypeQuality
all individuals: 1250
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5740
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1322
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1578
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1625
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 9.75e1
variant carriers: 7

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8748
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.184874234063442e-4
allele num: 59078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7874
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

FS
type: SiteQuality
SIO_000300: 6.037e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.126e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.123e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 1.283865e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

GenotypeQuality
all individuals: 1625
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1578
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7217
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36139
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7874
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8748
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15098
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59078
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.678668215253581e-5
allele num: 10332
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.126e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

DP
type: SiteQuality
SIO_000300: 1.283865e6

FS
type: SiteQuality
SIO_000300: 6.037e0

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

QD
type: SiteQuality
SIO_000300: 1.123e1

GenotypeQuality
all individuals: 442
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1863
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 36708
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1069
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 408
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1087
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1723
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 229
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6445
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 428
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6014
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 9.25e1
variant carriers: 2

Other
type: Population
allele count: 3
allele frequency: 3.8860103626943e-3
allele num: 772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.16608362485424e-4
allele num: 60030
num of homozygotes: 0

Latino
type: Population
allele count: 32
allele frequency: 3.036629341431011e-3
allele num: 10538
num of homozygotes: 1

South Asian
type: Population
allele count: 3
allele frequency: 1.964636542239686e-4
allele num: 15270
num of homozygotes: 0

African
type: Population
allele count: 494
allele frequency: 5.475504322766571e-2
allele num: 9022
num of homozygotes: 13

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7992
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4908
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.92e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

FS
type: SiteQuality
SIO_000300: 1.639e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.41e0

DP
type: SiteQuality
SIO_000300: 1.308734e6

QD
type: SiteQuality
SIO_000300: 1.348e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 6269
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1830
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36964
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2029
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9108
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.975124378109452e-4
allele num: 8040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15374
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.314837e6

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.722e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

FS
type: SiteQuality
SIO_000300: 3.515e0

VQSLOD
type: SiteQuality
SIO_000300: -1.013e0

MQ
type: SiteQuality
SIO_000300: 5.881e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-2

QD
type: SiteQuality
SIO_000300: 8.77e0

GenotypeQuality
all individuals: 451
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6792
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3884
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2064
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2316
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39093
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 583
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8362
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.264222503160556e-4
allele num: 15820
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.071117561683599e-5
allele num: 11024
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.96e-1

FS
type: SiteQuality
SIO_000300: 6.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

DP
type: SiteQuality
SIO_000300: 1.369835e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.53e-1

QD
type: SiteQuality
SIO_000300: 1.228e1

GenotypeQuality
all individuals: 313
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2467
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2926
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2211
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1574
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39965
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6982
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63830
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16034
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.758087201125176e-4
allele num: 5688
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.393797e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.817e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

FS
type: SiteQuality
SIO_000300: 6.767e0

VQSLOD
type: SiteQuality
SIO_000300: 4.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

QD
type: SiteQuality
SIO_000300: 1.237e1

MQRankSum
type: SiteQuality
SIO_000300: -7.94e-1

GenotypeQuality
all individuals: 1604
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7015
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2823
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2234
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39760
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2507
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16068
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564406620568818e-5
allele num: 63922
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.220000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -9.526e-1

QD
type: SiteQuality
SIO_000300: 7.22e0

MQRankSum
type: SiteQuality
SIO_000300: 8.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.395967e6

GenotypeQuality
all individuals: 2345
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 647
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5862
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9860
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.191183754333828e-5
allele num: 16152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64348
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e0

MQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

QD
type: SiteQuality
SIO_000300: 1.494e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.525e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 2.751e0

VQSLOD
type: SiteQuality
SIO_000300: 3.2e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 1.409897e6

GenotypeQuality
all individuals: 332
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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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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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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
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variant carriers: 0

GenotypeQuality
all individuals: 2710
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9932
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5962
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16228
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544878727019929e-5
allele num: 64730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11310
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.027e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.420512e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

QD
type: SiteQuality
SIO_000300: 5.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 7

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: 670
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variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.080680519961713e-4
allele num: 64774
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9936
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5964
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16240
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.125e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.131e1

FS
type: SiteQuality
SIO_000300: 2.983e0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-1

DP
type: SiteQuality
SIO_000300: 1.424126e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.6e-2

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 672
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variant carriers: 0

GenotypeQuality
all individuals: 2709
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.157635467980295e-5
allele num: 16240
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.300353356890459e-4
allele num: 11320
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5964
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.006441223832528e-4
allele num: 9936
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.424126e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.6e-2

QD
type: SiteQuality
SIO_000300: 1.131e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.125e0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 2.983e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e-1

GenotypeQuality
all individuals: 2778
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
all individuals: 280
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variant carriers: 0

GenotypeQuality
all individuals: 235
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variant carriers: 0

GenotypeQuality
all individuals: 272
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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
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 7454
bin: 6.75e1
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GenotypeQuality
all individuals: 691
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.639450994193208e-4
allele num: 11366
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.229823212913144e-4
allele num: 65050
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.072e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

DP
type: SiteQuality
SIO_000300: 1.43307e6

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 6.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.219e1

GenotypeQuality
all individuals: 1833
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 857
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 260
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variant carriers: 0

GenotypeQuality
all individuals: 110
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GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 697
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variant carriers: 0

GenotypeQuality
all individuals: 2804
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10062
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6140
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.068237604320078e-5
allele num: 65184
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.035e0

MQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

DP
type: SiteQuality
SIO_000300: 1.437226e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

QD
type: SiteQuality
SIO_000300: 1.003e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10098
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528818223513224e-5
allele num: 65410
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

MQ
type: SiteQuality
SIO_000300: 5.702e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.47e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.05e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.444273e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.71e-1

FS
type: SiteQuality
SIO_000300: 1.536e0

QD
type: SiteQuality
SIO_000300: 1.275e1

GenotypeQuality
all individuals: 131
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
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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
all individuals: 2893
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variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 9.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522255373561469e-5
allele num: 65692
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.942e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.183e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.453396e6

VQSLOD
type: SiteQuality
SIO_000300: -4.388e-1

FS
type: SiteQuality
SIO_000300: 3.695e0

QD
type: SiteQuality
SIO_000300: 1.046e1

MQRankSum
type: SiteQuality
SIO_000300: -1.536e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 132
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variant carriers: 0

GenotypeQuality
all individuals: 102
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GenotypeQuality
all individuals: 730
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GenotypeQuality
all individuals: 1926
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7757
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.715356458079135e-5
allele num: 11474
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.08198515995621e-5
allele num: 16442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65860
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.461529e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.139e1

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1935
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.704735376044568e-5
allele num: 11488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65958
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.6199e1

QD
type: SiteQuality
SIO_000300: 1.24e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.815e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.087e0

DP
type: SiteQuality
SIO_000300: 1.464844e6

MQRankSum
type: SiteQuality
SIO_000300: 8.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.179e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.149999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1950
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.540913631822723e-5
allele num: 66066
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.93e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

VQSLOD
type: SiteQuality
SIO_000300: -4.698e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.98e0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.93e-1

QD
type: SiteQuality
SIO_000300: 1.627e1

DP
type: SiteQuality
SIO_000300: 1.470158e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.04e-2

GenotypeQuality
all individuals: 129
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variant carriers: 0

GenotypeQuality
all individuals: 68
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1979
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variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
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: 16498
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.242e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

FS
type: SiteQuality
SIO_000300: 4.738e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.47877e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 757
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
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variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 25
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GenotypeQuality
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GenotypeQuality
all individuals: 400
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GenotypeQuality
all individuals: 71
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GenotypeQuality
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GenotypeQuality
all individuals: 7861
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GenotypeQuality
all individuals: 86
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GenotypeQuality
all individuals: 1981
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GenotypeQuality
all individuals: 84
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 767
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variant carriers: 0

GenotypeQuality
all individuals: 3033
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510209012927389e-5
allele num: 66216
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.18e-1

QD
type: SiteQuality
SIO_000300: 1.286e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.65e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

VQSLOD
type: SiteQuality
SIO_000300: 6.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.09e-1

DP
type: SiteQuality
SIO_000300: 1.4802e6

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 23
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508614187007815e-5
allele num: 66286
num of homozygotes: 0

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.318e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.38e-1

FS
type: SiteQuality
SIO_000300: 2.1817e1

VQSLOD
type: SiteQuality
SIO_000300: -3.247e0

DP
type: SiteQuality
SIO_000300: 1.481486e6

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.680542110358181e-5
allele num: 10330
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.240368306275745e-4
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66286
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.86e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

DP
type: SiteQuality
SIO_000300: 1.482367e6

FS
type: SiteQuality
SIO_000300: 3.193e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.87e-1

QD
type: SiteQuality
SIO_000300: 1.227e1

GenotypeQuality
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bin: 6.25e1
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
all individuals: 26
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GenotypeQuality
all individuals: 3060
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66366
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.34e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.975e1

BaseQRankSum
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.91e-1

ClippingRankSum
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DP
type: SiteQuality
SIO_000300: 1.484746e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11
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GenotypeQuality
all individuals: 208
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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South Asian
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allele num: 16510
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ReadPosRankSum
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SIO_000300: 3.07e-1

VQSLOD
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FS
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BaseQRankSum
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InbreedingCoeff
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QD
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MQ
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MQRankSum
type: SiteQuality
SIO_000300: 6.02e-1

ClippingRankSum
type: SiteQuality
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DP
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SIO_000300: 1.485691e6

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

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

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

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

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

Latino
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allele count: 2
allele frequency: 1.729206294310911e-4
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66450
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

MQ
type: SiteQuality
SIO_000300: 5.938e1

DP
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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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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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele frequency: 1.504845602841149e-5
allele num: 66452
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.34e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.62e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.981e1

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.515352197471403e-5
allele num: 66440
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 2.605e0

DP
type: SiteQuality
SIO_000300: 1.48688e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.023e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.88e0

QD
type: SiteQuality
SIO_000300: 1.166e1

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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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66460
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
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.473e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.501e0

DP
type: SiteQuality
SIO_000300: 1.486927e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e0

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

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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variant carriers: 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
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allele frequency: 6.938020351526364e-4
allele num: 8648
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504619180885318e-5
allele num: 66462
num of homozygotes: 0

African
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allele count: 0
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Other
type: Population
allele count: 0
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FS
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

Other
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East Asian
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European (Non-Finnish)
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allele num: 66468
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African
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South Asian
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European (Finnish)
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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MQ
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QD
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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num of homozygotes: 0

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

Latino
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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African
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allele frequency: 9.628345850182938e-5
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66490
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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FS
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MQ
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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SIO_000300: -1.0e-4

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

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

Other
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allele frequency: 0.0e0
allele num: 906
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: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66498
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European (Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
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ClippingRankSum
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FS
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MQRankSum
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VQSLOD
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QD
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MQ
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InbreedingCoeff
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BaseQRankSum
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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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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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African
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allele count: 3
allele frequency: 2.887391722810395e-4
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 3.007157033740302e-5
allele num: 66508
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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QD
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FS
type: SiteQuality
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ClippingRankSum
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MQRankSum
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SIO_000300: 4.37e-1

BaseQRankSum
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DP
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SIO_000300: 1.488185e6

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

Latino
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allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 6.056201550387597e-5
allele num: 16512
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66518
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
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SIO_000300: 1.488257e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e-1

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.442e1

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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variant carriers: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.013952369497234e-5
allele num: 66512
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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Other
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MQRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.953e1

QD
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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DP
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FS
type: SiteQuality
SIO_000300: 5.17e-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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variant carriers: 0

South Asian
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num of homozygotes: 0

Other
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African
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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FS
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DP
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MQ
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InbreedingCoeff
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MQRankSum
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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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Latino
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South Asian
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African
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East Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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allele num: 66508
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DP
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ReadPosRankSum
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QD
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MQ
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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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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African
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European (Non-Finnish)
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European (Finnish)
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Other
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Latino
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South Asian
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InbreedingCoeff
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QD
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FS
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VQSLOD
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MQ
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MQRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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Other
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ReadPosRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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MQ
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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QD
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MQRankSum
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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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variant carriers: 0

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

African
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num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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South Asian
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Latino
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VQSLOD
type: SiteQuality
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QD
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BaseQRankSum
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ClippingRankSum
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