4-171008245-TGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008245
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008243
    reference: chr 4
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.369+20_369+21delTC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.381+20_381+21delTC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.168+20_168+21delTC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.369+20_369+21delTC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.369+20_369+21delTC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.369+20_369+21delTC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.342+20_342+21delTC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.369+20_369+21delTC
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16102
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40305
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: TGA
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-171008245-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008245
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008244
    reference: chr 4
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.369+21delC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.381+21delC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.168+21delC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.342+21delC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.369+21delC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.369+21delC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.369+21delC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.369+21delC
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2090
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: TG
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

4-171008252-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008252
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008252
    reference: chr 4
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.369+15A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.369+15A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.342+15A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.369+15A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.369+15A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.369+15A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.381+15A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.168+15A>T
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2091
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

4-171008273-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008273
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008273
    reference: chr 4
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.363T>C
  hgvsp: ENST00000502392.1:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.162T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.363T>C
  hgvsp: ENST00000337664.4:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.363T>C
  hgvsp: ENST00000515480.1:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.363T>C
  hgvsp: ENST00000353187.2:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.375T>C
  hgvsp: ENST00000509167.1:c.375T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.363T>C
  hgvsp: ENST00000507375.1:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.336T>C
  hgvsp: ENST00000510340.1:c.336T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9485
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu121Leu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

4-171008282-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008282
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008282
    reference: chr 4
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.153A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.354A>G
  hgvsp: ENST00000507375.1:c.354A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.354A>G
  hgvsp: ENST00000502392.1:c.354A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.354A>G
  hgvsp: ENST00000353187.2:c.354A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.366A>G
  hgvsp: ENST00000509167.1:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.327A>G
  hgvsp: ENST00000510340.1:c.327A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.354A>G
  hgvsp: ENST00000337664.4:c.354A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.354A>G
  hgvsp: ENST00000515480.1:c.354A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4575
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Gln118Gln
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

4-171008285-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008285
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008285
    reference: chr 4
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.351C>T
  hgvsp: ENST00000353187.2:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.351C>T
  hgvsp: ENST00000515480.1:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.351C>T
  hgvsp: ENST00000507375.1:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.363C>T
  hgvsp: ENST00000509167.1:c.363C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.324C>T
  hgvsp: ENST00000510340.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.351C>T
  hgvsp: ENST00000502392.1:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.351C>T
  hgvsp: ENST00000337664.4:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.150C>T
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9486
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser117Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

4-171008295-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008295
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008295
    reference: chr 4
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.341C>T
  hgvsp: ENSP00000421389.1:p.Thr114Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.341C>T
  hgvsp: ENSP00000423843.1:p.Thr114Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.341C>T
  hgvsp: ENSP00000423341.1:p.Thr114Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.341C>T
  hgvsp: ENSP00000336808.4:p.Thr114Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.140C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.314C>T
  hgvsp: ENSP00000425067.1:p.Thr105Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.353C>T
  hgvsp: ENSP00000423190.1:p.Thr118Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.341C>T
  hgvsp: ENSP00000226840.4:p.Thr114Ile
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 28451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40317
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2090
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr114Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

4-171008303-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008303
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008303
    reference: chr 4
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.132A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.333A>T
  hgvsp: ENST00000515480.1:c.333A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.306A>T
  hgvsp: ENST00000510340.1:c.306A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.333A>T
  hgvsp: ENST00000353187.2:c.333A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.333A>T
  hgvsp: ENST00000337664.4:c.333A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.345A>T
  hgvsp: ENST00000509167.1:c.345A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.333A>T
  hgvsp: ENST00000507375.1:c.333A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.333A>T
  hgvsp: ENST00000502392.1:c.333A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4570
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu111Leu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS

4-171008303-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008303
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008303
    reference: chr 4
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.333A>G
  hgvsp: ENST00000353187.2:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.333A>G
  hgvsp: ENST00000507375.1:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.306A>G
  hgvsp: ENST00000510340.1:c.306A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.333A>G
  hgvsp: ENST00000337664.4:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.132A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.333A>G
  hgvsp: ENST00000502392.1:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.333A>G
  hgvsp: ENST00000515480.1:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.345A>G
  hgvsp: ENST00000509167.1:c.345A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu111Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

4-171008311-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008311
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008311
    reference: chr 4
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.337A>T
  hgvsp: ENSP00000423190.1:p.Met113Leu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.325A>T
  hgvsp: ENSP00000421389.1:p.Met109Leu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.325A>T
  hgvsp: ENSP00000226840.4:p.Met109Leu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.325A>T
  hgvsp: ENSP00000423843.1:p.Met109Leu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.298A>T
  hgvsp: ENSP00000425067.1:p.Met100Leu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.124A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.325A>T
  hgvsp: ENSP00000423341.1:p.Met109Leu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.325A>T
  hgvsp: ENSP00000336808.4:p.Met109Leu
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9487
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Met109Leu
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

4-171008318-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008318
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008318
    reference: chr 4
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.117A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.318A>G
  hgvsp: ENST00000502392.1:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.318A>G
  hgvsp: ENST00000337664.4:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.318A>G
  hgvsp: ENST00000353187.2:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.318A>G
  hgvsp: ENST00000515480.1:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.318A>G
  hgvsp: ENST00000507375.1:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.291A>G
  hgvsp: ENST00000510340.1:c.291A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.330A>G
  hgvsp: ENST00000509167.1:c.330A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4564
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40320
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2090
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln106Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

4-171008331-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008331
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008331
    reference: chr 4
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.305A>G
  hgvsp: ENSP00000226840.4:p.Tyr102Cys
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.104A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.305A>G
  hgvsp: ENSP00000336808.4:p.Tyr102Cys
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.278A>G
  hgvsp: ENSP00000425067.1:p.Tyr93Cys
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.305A>G
  hgvsp: ENSP00000423843.1:p.Tyr102Cys
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.305A>G
  hgvsp: ENSP00000423341.1:p.Tyr102Cys
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.305A>G
  hgvsp: ENSP00000421389.1:p.Tyr102Cys
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.317A>G
  hgvsp: ENSP00000423190.1:p.Tyr106Cys
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9488
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40322
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr102Cys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-171008354-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008354
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008354
    reference: chr 4
allele count: 27
allele frequency: 2.224162643952749e-4
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.282G>A
  hgvsp: ENST00000353187.2:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.282G>A
  hgvsp: ENST00000502392.1:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.282G>A
  hgvsp: ENST00000515480.1:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.282G>A
  hgvsp: ENST00000507375.1:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.282G>A
  hgvsp: ENST00000337664.4:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.81G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.294G>A
  hgvsp: ENST00000509167.1:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.255G>A
  hgvsp: ENST00000510340.1:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2087
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu94Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

4-171008366-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008366
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008366
    reference: chr 4
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.243A>G
  hgvsp: ENST00000510340.1:c.243A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.270A>G
  hgvsp: ENST00000507375.1:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.270A>G
  hgvsp: ENST00000502392.1:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.282A>G
  hgvsp: ENST00000509167.1:c.282A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.270A>G
  hgvsp: ENST00000337664.4:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.270A>G
  hgvsp: ENST00000353187.2:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.270A>G
  hgvsp: ENST00000515480.1:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.69A>G
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4542
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu90Leu
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP

4-171008405-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008405
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008405
    reference: chr 4
allele count: 2
allele frequency: 1.671933256424403e-5
allele num: 119622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-6C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-6C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-6C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-6C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-6C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-6C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-6C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-6C>T
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14687
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1961
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37948
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: c.237-6C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-171008406-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008406
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008407
    reference: chr 4
allele count: 1
allele frequency: 8.375349670848758e-6
allele num: 119398
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-8dupT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-8dupT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-8dupT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-8dupT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-8dupT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-8dupT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-8dupT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-8dupT
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4474
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
hgvs: c.237-8dupT
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/4-171008411-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008411
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008411
    reference: chr 4
allele count: 1
allele frequency: 8.432983083435934e-6
allele num: 118582
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-12T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-12T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-12T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-12T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-12T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-12T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-12T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-12T>G
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8521
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3995
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

4-171008414-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008414
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008414
    reference: chr 4
allele count: 1
allele frequency: 8.484498820654664e-6
allele num: 117862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-15C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-15C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-15C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-15C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-15C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-15C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-15C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-15C>T
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33624
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

4-171008415-T-TAGA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008415
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008418
    reference: chr 4
allele count: 2
allele frequency: 1.701027420562019e-5
allele num: 117576
alternate allele: TAGA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-17_210-16insTCT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-17_237-16insTCT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-17_237-16insTCT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-17_249-16insTCT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-17_237-16insTCT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-17_36-16insTCT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-17_237-16insTCT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-17_237-16insTCT
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6447
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32068
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7746
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1417
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-171008416-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008416
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008416
    reference: chr 4
allele count: 1
allele frequency: 8.505571149102662e-6
allele num: 117570
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-17T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-17T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-17T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-17T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-17T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-17T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-17T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-17T>G
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1419
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32407
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4468
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6180
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

4-171008416-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008416
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008416
    reference: chr 4
allele count: 1
allele frequency: 8.505571149102662e-6
allele num: 117570
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-17T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-17T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-17T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-17T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-17T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-17T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-17T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-17T>C
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1685
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7736
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32407
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

4-171008417-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008417
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008417
    reference: chr 4
allele count: 2
allele frequency: 1.709167977028783e-5
allele num: 117016
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-18A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-18A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-18A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-18A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-18A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-18A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-18A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-18A>C
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6775
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7489
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1733
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

4-171008417-T-TTGGAAGCATTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008417
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008428
    reference: chr 4
allele count: 2
allele frequency: 1.709167977028783e-5
allele num: 117016
alternate allele: TTGGAAGCATTC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1733
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1723
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7489
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-171008418-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008418
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008418
    reference: chr 4
allele count: 1
allele frequency: 8.54963920522554e-6
allele num: 116964
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-19T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-19T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-19T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-19T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-19T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-19T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-19T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-19T>G
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2119
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

4-171008419-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008419
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008419
    reference: chr 4
allele count: 2
allele frequency: 1.714560043892737e-5
allele num: 116648
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-20A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-20A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-20A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-20A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-20A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-20A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-20A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-20A>T
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9059
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6357
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4442
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1501
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6628
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: T
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

4-171008421-T-TGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008421
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008423
    reference: chr 4
allele count: 1
allele frequency: 8.563696776624533e-6
allele num: 116772
alternate allele: TGG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-23_237-22insCC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-23_237-22insCC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-23_237-22insCC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-23_249-22insCC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-23_237-22insCC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-23_237-22insCC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-23_36-22insCC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-23_210-22insCC
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9798
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2345
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1517
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4444
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
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: T
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

4-171008421-T-TGGAAGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008421
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008427
    reference: chr 4
allele count: 1
allele frequency: 8.563696776624533e-6
allele num: 116772
alternate allele: TGGAAGC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-23_237-22insGCTTCC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-23_237-22insGCTTCC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-23_237-22insGCTTCC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-23_210-22insGCTTCC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-23_249-22insGCTTCC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-23_237-22insGCTTCC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-23_36-22insGCTTCC
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-23_237-22insGCTTCC
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9798
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8366
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2345
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2723
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

4-171008428-ATAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008428
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008425
    reference: chr 4
allele count: 4
allele frequency: 3.457216940363008e-5
allele num: 115700
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-32_237-30delCTA
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-32_237-30delCTA
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-32_210-30delCTA
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-32_237-30delCTA
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-32_237-30delCTA
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-32_237-30delCTA
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-32_36-30delCTA
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-32_249-30delCTA
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16522
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7435
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10354
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2852
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5511
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20414
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: ATAG
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

4-171008444-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008444
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008444
    reference: chr 4
allele count: 2
allele frequency: 1.821792279244321e-5
allele num: 109782
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-45A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-45A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-45A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-45A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-45A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-45A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-45A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-45A>G
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13206
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15329
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3235
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7508
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8882
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2287
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-171008444-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008444
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008444
    reference: chr 4
allele count: 1
allele frequency: 9.108961396221603e-6
allele num: 109782
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-45A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-45A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-45A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-45A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-45A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-45A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-45A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-45A>C
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8141
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5043
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

4-171008446-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008446
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008446
    reference: chr 4
allele count: 1
allele frequency: 9.100837277029487e-6
allele num: 109880
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-47C>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-47C>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-47C>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-47C>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-47C>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-47C>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-47C>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-47C>G
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9077
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4763
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1198
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1050
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

4-171008447-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008447
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008447
    reference: chr 4
allele count: 2
allele frequency: 1.817686085613014e-5
allele num: 110030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-48A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-48A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-48A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-48A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-48A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-48A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-48A>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-48A>T
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4483
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13270
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10321
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1200
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2053
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9233
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4582
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-171008450-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171008450
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171008450
    reference: chr 4
allele count: 1
allele frequency: 9.355412105903265e-6
allele num: 106890
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.210-51G>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.237-51G>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.36-51G>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.237-51G>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.237-51G>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.249-51G>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.237-51G>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.237-51G>C
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15097
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1375
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1892
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7529
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4433
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1088
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1165
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

4-171009498-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009498
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009498
    reference: chr 4
allele count: 1
allele frequency: 8.483491126268282e-6
allele num: 117876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.236+49A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.209+49A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.248+49A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.236+49A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.236+49A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.236+49A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.236+49A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.35+49A>G
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7751
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9753
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1685
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4382
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1215
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2514
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4332
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3883
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

4-171009506-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009506
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009505
    reference: chr 4
allele count: 1
allele frequency: 8.47860001356576e-6
allele num: 117944
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.236+40delT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.35+40delT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.236+40delT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.209+40delT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.236+40delT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.236+40delT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.236+40delT
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.248+40delT
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7797
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4284
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4362
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1445
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: GA
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

4-171009531-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009531
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009531
    reference: chr 4
allele count: 6
allele frequency: 5.016219108450657e-5
allele num: 119612
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.236+16T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.209+16T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.236+16T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.35+16T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.236+16T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.236+16T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.236+16T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.248+16T>C
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4805
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-171009532-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009532
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009532
    reference: chr 4
allele count: 4
allele frequency: 3.340571237681643e-5
allele num: 119740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.248+15T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.236+15T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.236+15T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.209+15T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.35+15T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.236+15T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.236+15T>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.236+15T>G
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22889
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2635
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP

4-171009536-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009536
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009536
    reference: chr 4
allele count: 1
allele frequency: 8.318360284820657e-6
allele num: 120216
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.236+11A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.236+11A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.236+11A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.248+11A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.35+11A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.236+11A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.236+11A>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.209+11A>C
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4491
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4544
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

4-171009538-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009538
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009538
    reference: chr 4
allele count: 2
allele frequency: 1.661019201381968e-5
allele num: 120408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.35+9C>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.209+9C>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.236+9C>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.236+9C>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.236+9C>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.236+9C>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.248+9C>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.236+9C>A
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7893
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2649
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13692
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4541
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

4-171009539-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009539
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009539
    reference: chr 4
allele count: 1
allele frequency: 8.29737802854298e-6
allele num: 120520
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.236+8T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.236+8T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.35+8T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.248+8T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.209+8T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.236+8T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.236+8T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.236+8T>C
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22903
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4022
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.75e1
  variant carriers: 0
hgvs: c.236+8T>C
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

4-171009551-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009551
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009551
    reference: chr 4
allele count: 1
allele frequency: 8.25559316436886e-6
allele num: 121130
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.244G>C
  hgvsp: ENSP00000423190.1:p.Ala82Pro
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.232G>C
  hgvsp: ENSP00000423341.1:p.Ala78Pro
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.232G>C
  hgvsp: ENSP00000421389.1:p.Ala78Pro
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.205G>C
  hgvsp: ENSP00000425067.1:p.Ala69Pro
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.31G>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.232G>C
  hgvsp: ENSP00000226840.4:p.Ala78Pro
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.232G>C
  hgvsp: ENSP00000336808.4:p.Ala78Pro
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.232G>C
  hgvsp: ENSP00000423843.1:p.Ala78Pro
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2663
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4552
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4025
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala78Pro
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

4-171009555-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009555
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009555
    reference: chr 4
allele count: 5
allele frequency: 4.125276393518366e-5
allele num: 121204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.228G>A
  hgvsp: ENST00000353187.2:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.27G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.228G>A
  hgvsp: ENST00000502392.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.228G>A
  hgvsp: ENST00000507375.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.228G>A
  hgvsp: ENST00000337664.4:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.201G>A
  hgvsp: ENST00000510340.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.228G>A
  hgvsp: ENST00000515480.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.240G>A
  hgvsp: ENST00000509167.1:c.240G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2664
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro76Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP

4-171009556-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009556
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009556
    reference: chr 4
allele count: 3
allele frequency: 2.474349246148263e-5
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.26C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.227C>T
  hgvsp: ENSP00000423843.1:p.Pro76Leu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.227C>T
  hgvsp: ENSP00000336808.4:p.Pro76Leu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.200C>T
  hgvsp: ENSP00000425067.1:p.Pro67Leu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.239C>T
  hgvsp: ENSP00000423190.1:p.Pro80Leu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.227C>T
  hgvsp: ENSP00000423341.1:p.Pro76Leu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.227C>T
  hgvsp: ENSP00000226840.4:p.Pro76Leu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.227C>T
  hgvsp: ENSP00000421389.1:p.Pro76Leu
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2664
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22911
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2406
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro76Leu
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

4-171009564-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009564
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009564
    reference: chr 4
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.231G>A
  hgvsp: ENST00000509167.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.219G>A
  hgvsp: ENST00000507375.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.219G>A
  hgvsp: ENST00000502392.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.219G>A
  hgvsp: ENST00000337664.4:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.192G>A
  hgvsp: ENST00000510340.1:c.192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.219G>A
  hgvsp: ENST00000515480.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.219G>A
  hgvsp: ENST00000353187.2:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.18G>A
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4556
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2663
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14503
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4508
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln73Gln
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

4-171009570-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009570
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009570
    reference: chr 4
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.213A>G
  hgvsp: ENST00000353187.2:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.213A>G
  hgvsp: ENST00000502392.1:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.213A>G
  hgvsp: ENST00000515480.1:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.213A>G
  hgvsp: ENST00000507375.1:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.225A>G
  hgvsp: ENST00000509167.1:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.213A>G
  hgvsp: ENST00000337664.4:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109576
  ensembl transcript: ENST00000505906
  gene symbol: AADAT
  hgvsc: ENST00000505906.1:n.12A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.186A>G
  hgvsp: ENST00000510340.1:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10670
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4512
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22914
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala71Ala
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

4-171009587-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009587
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009587
    reference: chr 4
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.169G>C
  hgvsp: ENSP00000425067.1:p.Glu57Gln
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.208G>C
  hgvsp: ENSP00000423190.1:p.Glu70Gln
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.196G>C
  hgvsp: ENSP00000336808.4:p.Glu66Gln
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.196G>C
  hgvsp: ENSP00000423341.1:p.Glu66Gln
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.196G>C
  hgvsp: ENSP00000421389.1:p.Glu66Gln
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.196G>C
  hgvsp: ENSP00000226840.4:p.Glu66Gln
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.196G>C
  hgvsp: ENSP00000423843.1:p.Glu66Gln
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22916
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4999
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4025
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu66Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-171009595-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009595
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009595
    reference: chr 4
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.188T>C
  hgvsp: ENSP00000423843.1:p.Phe63Ser
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.188T>C
  hgvsp: ENSP00000226840.4:p.Phe63Ser
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.188T>C
  hgvsp: ENSP00000336808.4:p.Phe63Ser
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.200T>C
  hgvsp: ENSP00000423190.1:p.Phe67Ser
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.188T>C
  hgvsp: ENSP00000423341.1:p.Phe63Ser
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.188T>C
  hgvsp: ENSP00000421389.1:p.Phe63Ser
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.161T>C
  hgvsp: ENSP00000425067.1:p.Phe54Ser
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2662
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5000
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Phe63Ser
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

4-171009599-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009599
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009599
    reference: chr 4
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.184C>A
  hgvsp: ENSP00000423843.1:p.Gln62Lys
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.196C>A
  hgvsp: ENSP00000423190.1:p.Gln66Lys
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.184C>A
  hgvsp: ENSP00000336808.4:p.Gln62Lys
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.184C>A
  hgvsp: ENSP00000421389.1:p.Gln62Lys
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.184C>A
  hgvsp: ENSP00000226840.4:p.Gln62Lys
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.184C>A
  hgvsp: ENSP00000423341.1:p.Gln62Lys
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.157C>A
  hgvsp: ENSP00000425067.1:p.Gln53Lys
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4512
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22914
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2661
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln62Lys
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

4-171009628-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009628
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009628
    reference: chr 4
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.155T>C
  hgvsp: ENSP00000423843.1:p.Val52Ala
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.167T>C
  hgvsp: ENSP00000423190.1:p.Val56Ala
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.155T>C
  hgvsp: ENSP00000336808.4:p.Val52Ala
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.155T>C
  hgvsp: ENSP00000421389.1:p.Val52Ala
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.155T>C
  hgvsp: ENSP00000423341.1:p.Val52Ala
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.155T>C
  hgvsp: ENSP00000226840.4:p.Val52Ala
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.128T>C
  hgvsp: ENSP00000425067.1:p.Val43Ala
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22914
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4555
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4997
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2663
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4025
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val52Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum

4-171009629-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009629
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009629
    reference: chr 4
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.154G>A
  hgvsp: ENSP00000226840.4:p.Val52Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.127G>A
  hgvsp: ENSP00000425067.1:p.Val43Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.166G>A
  hgvsp: ENSP00000423190.1:p.Val56Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.154G>A
  hgvsp: ENSP00000423341.1:p.Val52Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.154G>A
  hgvsp: ENSP00000423843.1:p.Val52Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.154G>A
  hgvsp: ENSP00000336808.4:p.Val52Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.154G>A
  hgvsp: ENSP00000421389.1:p.Val52Ile
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4513
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22914
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4555
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4025
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val52Ile
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

4-171009630-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009630
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009630
    reference: chr 4
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.165C>T
  hgvsp: ENST00000509167.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.126C>T
  hgvsp: ENST00000510340.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.153C>T
  hgvsp: ENST00000353187.2:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.153C>T
  hgvsp: ENST00000337664.4:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.153C>T
  hgvsp: ENST00000507375.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.153C>T
  hgvsp: ENST00000502392.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.153C>T
  hgvsp: ENST00000515480.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14612
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala51Ala
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD

4-171009649-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009649
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009649
    reference: chr 4
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.146T>C
  hgvsp: ENSP00000423190.1:p.Met49Thr
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.134T>C
  hgvsp: ENSP00000336808.4:p.Met45Thr
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.134T>C
  hgvsp: ENSP00000421389.1:p.Met45Thr
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.134T>C
  hgvsp: ENSP00000423341.1:p.Met45Thr
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.134T>C
  hgvsp: ENSP00000226840.4:p.Met45Thr
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.134T>C
  hgvsp: ENSP00000423843.1:p.Met45Thr
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.107T>C
  hgvsp: ENSP00000425067.1:p.Met36Thr
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2662
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22915
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14613
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2408
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met45Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

4-171009671-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009671
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009671
    reference: chr 4
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.112G>A
  hgvsp: ENSP00000226840.4:p.Gly38Ser
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.112G>A
  hgvsp: ENSP00000421389.1:p.Gly38Ser
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.112G>A
  hgvsp: ENSP00000423341.1:p.Gly38Ser
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.124G>A
  hgvsp: ENSP00000423190.1:p.Gly42Ser
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.112G>A
  hgvsp: ENSP00000423843.1:p.Gly38Ser
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.112G>A
  hgvsp: ENSP00000336808.4:p.Gly38Ser
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.85G>A
  hgvsp: ENSP00000425067.1:p.Gly29Ser
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14590
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4511
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly38Ser
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

4-171009679-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009679
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009679
    reference: chr 4
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.104C>T
  hgvsp: ENSP00000421389.1:p.Ser35Phe
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.104C>T
  hgvsp: ENSP00000226840.4:p.Ser35Phe
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.104C>T
  hgvsp: ENSP00000423341.1:p.Ser35Phe
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.116C>T
  hgvsp: ENSP00000423190.1:p.Ser39Phe
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.104C>T
  hgvsp: ENSP00000336808.4:p.Ser35Phe
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.77C>T
  hgvsp: ENSP00000425067.1:p.Ser26Phe
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.104C>T
  hgvsp: ENSP00000423843.1:p.Ser35Phe
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14554
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4511
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser35Phe
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/4-171009684-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009684
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009684
    reference: chr 4
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.111G>T
  hgvsp: ENSP00000423190.1:p.Met37Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.99G>T
  hgvsp: ENSP00000423843.1:p.Met33Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.72G>T
  hgvsp: ENSP00000425067.1:p.Met24Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.99G>T
  hgvsp: ENSP00000421389.1:p.Met33Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.99G>T
  hgvsp: ENSP00000423341.1:p.Met33Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.99G>T
  hgvsp: ENSP00000336808.4:p.Met33Ile
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.99G>T
  hgvsp: ENSP00000226840.4:p.Met33Ile
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4986
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4509
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14528
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4023
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Met33Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

4-171009687-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009687
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009687
    reference: chr 4
allele count: 6
allele frequency: 4.94600610007419e-5
allele num: 121310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.108G>A
  hgvsp: ENST00000509167.1:c.108G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.96G>A
  hgvsp: ENST00000502392.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.96G>A
  hgvsp: ENST00000353187.2:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.69G>A
  hgvsp: ENST00000510340.1:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.96G>A
  hgvsp: ENST00000337664.4:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.96G>A
  hgvsp: ENST00000515480.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.96G>A
  hgvsp: ENST00000507375.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14505
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2653
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22918
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser32Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS

4-171009690-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009690
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009690
    reference: chr 4
allele count: 2
allele frequency: 1.648723063986942e-5
allele num: 121306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.105A>G
  hgvsp: ENST00000509167.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.93A>G
  hgvsp: ENST00000502392.1:c.93A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.66A>G
  hgvsp: ENST00000510340.1:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.93A>G
  hgvsp: ENST00000507375.1:c.93A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.93A>G
  hgvsp: ENST00000337664.4:c.93A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.93A>G
  hgvsp: ENST00000353187.2:c.93A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.93A>G
  hgvsp: ENST00000515480.1:c.93A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2652
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4984
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys31Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

4-171009707-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009707
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009707
    reference: chr 4
allele count: 2
allele frequency: 1.649756660892518e-5
allele num: 121230
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.49T>C
  hgvsp: ENST00000510340.1:c.49T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.76T>C
  hgvsp: ENST00000507375.1:c.76T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.76T>C
  hgvsp: ENST00000502392.1:c.76T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.76T>C
  hgvsp: ENST00000337664.4:c.76T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.76T>C
  hgvsp: ENST00000515480.1:c.76T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.76T>C
  hgvsp: ENST00000353187.2:c.76T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.88T>C
  hgvsp: ENST00000509167.1:c.88T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10675
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4961
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4552
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu26Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

4-171009711-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009711
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009711
    reference: chr 4
allele count: 2
allele frequency: 1.650464605786529e-5
allele num: 121178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.84C>A
  hgvsp: ENSP00000423190.1:p.Asp28Glu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.72C>A
  hgvsp: ENSP00000336808.4:p.Asp24Glu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.72C>A
  hgvsp: ENSP00000423341.1:p.Asp24Glu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.72C>A
  hgvsp: ENSP00000226840.4:p.Asp24Glu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.72C>A
  hgvsp: ENSP00000423843.1:p.Asp24Glu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.72C>A
  hgvsp: ENSP00000421389.1:p.Asp24Glu
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.45C>A
  hgvsp: ENSP00000425067.1:p.Asp15Glu
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp24Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

4-171009719-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009719
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009719
    reference: chr 4
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.68-4G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.68-4G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.41-4G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.80-4G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.68-4G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.68-4G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.68-4G>A
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2406
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2636
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4023
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14195
  bin: 6.25e1
  variant carriers: 0
hgvs: c.68-4G>A
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

4-171009726-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009726
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009726
    reference: chr 4
allele count: 1
allele frequency: 8.267059076404159e-6
allele num: 120962
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.68-11G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.68-11G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.68-11G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.68-11G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.68-11G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.80-11G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.41-11G>A
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13227
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7893
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4909
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4549
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13854
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4489
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

4-171009727-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009727
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009727
    reference: chr 4
allele count: 1
allele frequency: 8.268836409340477e-6
allele num: 120936
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.68-12T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.41-12T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.68-12T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.68-12T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.80-12T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.68-12T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.68-12T>C
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7888
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4490
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4024
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

4-171009734-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009734
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009734
    reference: chr 4
allele count: 1
allele frequency: 8.272803984182399e-6
allele num: 120878
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.68-19T>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.68-19T>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.80-19T>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.68-19T>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.41-19T>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.68-19T>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.68-19T>A
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7887
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2627
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4486
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4870
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD

4-171009735-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009735
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009735
    reference: chr 4
allele count: 4
allele frequency: 3.309285856112251e-5
allele num: 120872
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.68-20C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.68-20C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.68-20C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.41-20C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.80-20C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.68-20C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.68-20C>T
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7888
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4865
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/4-171009742-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009742
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009742
    reference: chr 4
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.80-27G>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.68-27G>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.68-27G>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.41-27G>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.68-27G>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.68-27G>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.68-27G>T
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7888
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4545
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4835
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2618
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4477
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22916
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

4-171009750-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009750
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009750
    reference: chr 4
allele count: 46
allele frequency: 3.81198621055423e-4
allele num: 120672
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.68-35A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.68-35A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.80-35A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.68-35A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.68-35A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.68-35A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.41-35A>G
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10747
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10542
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11479
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 22944
  bin: 9.75e1
  variant carriers: 45
genotype quality: GenotypeQuality
  all individuals: 4751
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4468
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4020
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11428
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4539
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

4-171009756-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009756
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009756
    reference: chr 4
allele count: 1
allele frequency: 8.292011476143882e-6
allele num: 120598
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.68-41T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.41-41T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.80-41T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.68-41T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.68-41T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.68-41T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.68-41T>C
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10813
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4716
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2600
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP

4-171009761-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009761
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009761
    reference: chr 4
allele count: 1
allele frequency: 8.305647840531562e-6
allele num: 120400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.68-46A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.80-46A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.68-46A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.68-46A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.41-46A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.68-46A>G
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.68-46A>G
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4613
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2587
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

4-171009762-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009762
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009762
    reference: chr 4
allele count: 1
allele frequency: 8.305785810395521e-6
allele num: 120398
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.68-47T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.68-47T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.68-47T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.68-47T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.80-47T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.68-47T>C
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.41-47T>C
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22922
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

4-171009766-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009766
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009766
    reference: chr 4
allele count: 2
allele frequency: 1.662040653514385e-5
allele num: 120334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.68-51C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.68-51C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.80-51C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.41-51C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.68-51C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.68-51C>T
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.68-51C>T
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7877
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4597
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8507
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2587
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD

4-171009767-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171009767
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 171009767
    reference: chr 4
allele count: 2
allele frequency: 1.664890783164624e-5
allele num: 120128
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000425067
  ensembl transcript: ENST00000510340
  gene symbol: AADAT
  hgvsc: ENST00000510340.1:c.41-52G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423341
  ensembl transcript: ENST00000515480
  gene symbol: AADAT
  hgvsc: ENST00000515480.1:c.68-52G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000421389
  ensembl transcript: ENST00000507375
  gene symbol: AADAT
  hgvsc: ENST00000507375.1:c.68-52G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000336808
  ensembl transcript: ENST00000337664
  gene symbol: AADAT
  hgvsc: ENST00000337664.4:c.68-52G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423843
  ensembl transcript: ENST00000502392
  gene symbol: AADAT
  hgvsc: ENST00000502392.1:c.68-52G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000226840
  ensembl transcript: ENST00000353187
  gene symbol: AADAT
  hgvsc: ENST00000353187.2:c.68-52G>A
  variant of: http://identifiers.org/hgnc/17929
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109576
  ensembl protein: ENSP00000423190
  ensembl transcript: ENST00000509167
  gene symbol: AADAT
  hgvsc: ENST00000509167.1:c.80-52G>A
  variant of: http://identifiers.org/hgnc/17929
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7881
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 882
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8121
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2582
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1279
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22920
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
reference allele: C

GenotypeQuality
all individuals: 710
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1094
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2090
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 447
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9485
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4579
bin: 9.75e1
variant carriers: 1

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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European (Non-Finnish)
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QD
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BaseQRankSum
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MQ
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DP
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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East Asian
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European (Non-Finnish)
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African
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South Asian
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Other
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FS
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InbreedingCoeff
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MQ
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DP
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QD
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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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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FS
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InbreedingCoeff
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ClippingRankSum
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Finnish)
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South Asian
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European (Non-Finnish)
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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QD
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DP
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ClippingRankSum
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FS
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MQ
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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Latino
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South Asian
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African
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European (Non-Finnish)
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MQRankSum
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ClippingRankSum
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QD
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MQ
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BaseQRankSum
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InbreedingCoeff
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FS
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DP
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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South Asian
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Other
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African
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European (Non-Finnish)
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DP
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ReadPosRankSum
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VQSLOD
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FS
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BaseQRankSum
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QD
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MQ
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InbreedingCoeff
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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Latino
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South Asian
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DP
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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FS
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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DP
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ClippingRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQRankSum
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QD
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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InbreedingCoeff
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FS
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DP
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ClippingRankSum
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QD
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.17e0

QD
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
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MQRankSum
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SIO_000300: 4.82e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.9e-2

DP
type: SiteQuality
SIO_000300: 1.969539e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e-1

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: -1.182e0

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
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FS
type: SiteQuality
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DP
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 66730
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

African
type: Population
allele count: 27
allele frequency: 2.594656928694984e-3
allele num: 10406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.35e-1

FS
type: SiteQuality
SIO_000300: 2.339e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.18e0

DP
type: SiteQuality
SIO_000300: 1.969485e6

VQSLOD
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QD
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SIO_000300: 1.268e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: 3.98e0

QD
type: SiteQuality
SIO_000300: 1.381e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.03e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.966758e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2
allele frequency: 3.0507337014552e-5
allele num: 65558
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-1

FS
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 902
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East Asian
type: Population
allele count: 1
allele frequency: 1.171234481143125e-4
allele num: 8538
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65448
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

Latino
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allele count: 0
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num of homozygotes: 0

InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
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QD
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MQ
type: SiteQuality
SIO_000300: 3.927e1

FS
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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DP
type: SiteQuality
SIO_000300: 1.896001e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
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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 frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.540357362908195e-5
allele num: 64920
num of homozygotes: 0

South Asian
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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QD
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MQRankSum
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VQSLOD
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ClippingRankSum
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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African
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allele frequency: 0.0e0
allele num: 10000
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European (Non-Finnish)
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European (Finnish)
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Latino
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East Asian
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South Asian
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ReadPosRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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DP
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.108292925525301e-5
allele num: 64344
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16080
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9970
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.248e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.482e0

QD
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 4.993e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.875e0

DP
type: SiteQuality
SIO_000300: 1.781731e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.47e-1

GenotypeQuality
all individuals: 646
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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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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variant carriers: 0

GenotypeQuality
all individuals: 142
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GenotypeQuality
all individuals: 386
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16074
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5542913985514e-5
allele num: 64338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9976
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

FS
type: SiteQuality
SIO_000300: 1.798e0

DP
type: SiteQuality
SIO_000300: 1.781006e6

MQ
type: SiteQuality
SIO_000300: 3.474e1

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

QD
type: SiteQuality
SIO_000300: 2.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1481
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.798169980644026e-5
allele num: 11366
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9976
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64338
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16074
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

DP
type: SiteQuality
SIO_000300: 1.781006e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

FS
type: SiteQuality
SIO_000300: 1.798e0

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

MQ
type: SiteQuality
SIO_000300: 3.474e1

VQSLOD
type: SiteQuality
SIO_000300: -3.02e-1

QD
type: SiteQuality
SIO_000300: 2.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15970
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.201056930098487e-4
allele num: 8326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64006
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.005025125628141e-4
allele num: 9950
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0876e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.244e0

DP
type: SiteQuality
SIO_000300: 1.760352e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 4.993e1

VQSLOD
type: SiteQuality
SIO_000300: -2.17e0

MQRankSum
type: SiteQuality
SIO_000300: -1.736e0

QD
type: SiteQuality
SIO_000300: 1.66e0

GenotypeQuality
all individuals: 374
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
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GenotypeQuality
all individuals: 6775
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 636
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variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15970
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.124707058713245e-5
allele num: 64006
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9950
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.17e0

DP
type: SiteQuality
SIO_000300: 1.760352e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.244e0

FS
type: SiteQuality
SIO_000300: 1.0876e1

QD
type: SiteQuality
SIO_000300: 1.66e0

MQRankSum
type: SiteQuality
SIO_000300: -1.736e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 4.993e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

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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variant carriers: 1

GenotypeQuality
all individuals: 945
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variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11336
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15990
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.563135023603339e-5
allele num: 63974
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.728e1

FS
type: SiteQuality
SIO_000300: 1.405e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 1.94e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

DP
type: SiteQuality
SIO_000300: 1.714474e6

VQSLOD
type: SiteQuality
SIO_000300: -1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.25e0

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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bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.20627261761158e-4
allele num: 8290
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15930
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63778
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.009489198465576e-4
allele num: 9906
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.993e1

FS
type: SiteQuality
SIO_000300: 4.304e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

VQSLOD
type: SiteQuality
SIO_000300: -3.26e0

MQRankSum
type: SiteQuality
SIO_000300: -1.231e0

DP
type: SiteQuality
SIO_000300: 1.712993e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.585e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63860
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9912
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.206563706563707e-4
allele num: 8288
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15964
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.953e-1

FS
type: SiteQuality
SIO_000300: 2.268e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQ
type: SiteQuality
SIO_000300: 4.907e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 1.691757e6

MQRankSum
type: SiteQuality
SIO_000300: -2.663e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.096e0

QD
type: SiteQuality
SIO_000300: 1.43e0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63860
num of homozygotes: 0

African
type: Population
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allele frequency: 1.008878127522195e-4
allele num: 9912
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8288
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

VQSLOD
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QD
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 1.31e0

ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 1.691757e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1362
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8212
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.330716637123322e-5
allele num: 63184
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.164999999999999e0

DP
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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MQ
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SIO_000300: 5.661e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

ClippingRankSum
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SIO_000300: -1.064e0

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 9350
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

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

Latino
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allele frequency: 9.199632014719411e-5
allele num: 10870
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.676333523317799e-5
allele num: 59654
num of homozygotes: 0

MQ
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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BaseQRankSum
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QD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.05e-1

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

South Asian
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allele count: 1
allele frequency: 6.69254450542096e-5
allele num: 14942
num of homozygotes: 0

Other
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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: 9350
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10870
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59654
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: 2.93e0

VQSLOD
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FS
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SIO_000300: 4.845e0

MQ
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ClippingRankSum
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MQRankSum
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SIO_000300: 9.22e-1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

DP
type: SiteQuality
SIO_000300: 1.405351e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.05e-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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9354
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.296008294453084e-4
allele num: 7716
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59678
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10884
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele num: 850
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.27e-1

MQ
type: SiteQuality
SIO_000300: 5.834e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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MQRankSum
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SIO_000300: 4.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.03e-1

DP
type: SiteQuality
SIO_000300: 1.403831e6

QD
type: SiteQuality
SIO_000300: 6.68e0

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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bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.346832223300646e-5
allele num: 59758
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15008
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.003e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

DP
type: SiteQuality
SIO_000300: 1.403365e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.723543605653223e-5
allele num: 58020
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6334
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10628
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
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DP
type: SiteQuality
SIO_000300: 1.396077e6

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 7.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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VQSLOD
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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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variant carriers: 1

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.521977352976988e-5
allele num: 65704
num of homozygotes: 0

East Asian
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allele count: 0
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num of homozygotes: 0

QD
type: SiteQuality
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DP
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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MQRankSum
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FS
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MQ
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.81e-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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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14510
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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Other
type: Population
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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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.52151421094273e-5
allele num: 65724
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.026e1

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.550588945937783e-5
allele num: 66220
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African
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South Asian
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European (Finnish)
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East Asian
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Latino
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allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.047777441790142e-4
allele num: 6614
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66244
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.201e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.85e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.087e0

DP
type: SiteQuality
SIO_000300: 2.151041e6

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2406
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507159005275056e-5
allele num: 66350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15794
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

FS
type: SiteQuality
SIO_000300: 6.607e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.41e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

DP
type: SiteQuality
SIO_000300: 2.156726e6

QD
type: SiteQuality
SIO_000300: 1.64e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4019
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.012320390396723e-5
allele num: 66394
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15930
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.299999999999999e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.15e-1

QD
type: SiteQuality
SIO_000300: 1.028e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.15e-1

DP
type: SiteQuality
SIO_000300: 2.159777e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.693e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15984
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.643201542912247e-5
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66446
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.764e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.38e0

DP
type: SiteQuality
SIO_000300: 2.160782e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.675e0

VQSLOD
type: SiteQuality
SIO_000300: -9.65e-2

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.10798924993892e-5
allele num: 16372
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.664e0

MQ
type: SiteQuality
SIO_000300: 5.873e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.456e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

DP
type: SiteQuality
SIO_000300: 2.170762e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.787e0

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

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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variant carriers: 5

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

FS
type: SiteQuality
SIO_000300: 6.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.949e0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.143e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.139999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.172455e6

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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bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.079766536964981e-5
allele num: 16448
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.182e1

FS
type: SiteQuality
SIO_000300: 1.781e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.928e1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.29e-1

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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variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

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

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 904
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
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.6e-2

DP
type: SiteQuality
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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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bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.832e0

BaseQRankSum
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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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European (Finnish)
type: Population
allele count: 0
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Latino
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European (Non-Finnish)
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African
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East Asian
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Other
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MQ
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ClippingRankSum
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MQRankSum
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DP
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VQSLOD
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QD
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InbreedingCoeff
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FS
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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VQSLOD
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InbreedingCoeff
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MQ
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FS
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ClippingRankSum
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MQRankSum
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QD
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ReadPosRankSum
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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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African
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Other
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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ReadPosRankSum
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FS
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BaseQRankSum
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MQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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African
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East Asian
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European (Non-Finnish)
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Other
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QD
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MQ
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FS
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DP
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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QD
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MQ
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MQRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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InbreedingCoeff
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ClippingRankSum
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DP
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VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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BaseQRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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Other
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East Asian
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Latino
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African
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VQSLOD
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DP
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ClippingRankSum
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QD
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InbreedingCoeff
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MQ
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BaseQRankSum
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FS
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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QD
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MQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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South Asian
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European (Finnish)
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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DP
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QD
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ReadPosRankSum
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VQSLOD
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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SIO_000300: -1.11e-1

QD
type: SiteQuality
SIO_000300: 1.231e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.642e0

FS
type: SiteQuality
SIO_000300: 4.549e0

VQSLOD
type: SiteQuality
SIO_000300: 6.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4508
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4554
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

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

African
type: Population
allele count: 6
allele frequency: 5.780346820809249e-4
allele num: 10380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

QD
type: SiteQuality
SIO_000300: 1.294e1

DP
type: SiteQuality
SIO_000300: 2.174636e6

FS
type: SiteQuality
SIO_000300: 5.31e-1

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999760019198464e-5
allele num: 66672
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.86e-1

DP
type: SiteQuality
SIO_000300: 2.174325e6

MQ
type: SiteQuality
SIO_000300: 5.938e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

FS
type: SiteQuality
SIO_000300: 1.736e0

QD
type: SiteQuality
SIO_000300: 1.4e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4495
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.18e-1

DP
type: SiteQuality
SIO_000300: 2.172472e6

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

FS
type: SiteQuality
SIO_000300: 4.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.8e-2

MQ
type: SiteQuality
SIO_000300: 5.952e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.25e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4953
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.93012931866435e-4
allele num: 10362
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.171895e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

VQSLOD
type: SiteQuality
SIO_000300: 8.99e-1

FS
type: SiteQuality
SIO_000300: 1.658e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 1.217e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.339e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.13e-1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4550
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4492
bin: 7.75e1
variant carriers: 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: 6.091617933723197e-5
allele num: 16416
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -7.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.69e-1

DP
type: SiteQuality
SIO_000300: 2.170169e6

FS
type: SiteQuality
SIO_000300: 2.084e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.524e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.72e-1

QD
type: SiteQuality
SIO_000300: 1.44e1

GenotypeQuality
all individuals: 2406
bin: 8.75e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 458
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.11545988258317e-5
allele num: 16352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66530
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.783e0

FS
type: SiteQuality
SIO_000300: 8.349e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.166535e6

VQSLOD
type: SiteQuality
SIO_000300: -1.836e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

MQRankSum
type: SiteQuality
SIO_000300: -7.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.965e0

QD
type: SiteQuality
SIO_000300: 7.79e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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bin: 9.75e1
variant carriers: 1

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: 10348
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66516
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.932e1

DP
type: SiteQuality
SIO_000300: 2.165206e6

FS
type: SiteQuality
SIO_000300: 5.643e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.97e-1

QD
type: SiteQuality
SIO_000300: 1.607e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.98e-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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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66496
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.669309611293753e-5
allele num: 10342
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

VQSLOD
type: SiteQuality
SIO_000300: -1.845e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.476e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

DP
type: SiteQuality
SIO_000300: 2.161312e6

FS
type: SiteQuality
SIO_000300: 1.2318e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.952999999999999e0

QD
type: SiteQuality
SIO_000300: 1.19e1

GenotypeQuality
all individuals: 35
bin: 4.25e1
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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GenotypeQuality
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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: 4

African
type: Population
allele count: 2
allele frequency: 1.933861922258751e-4
allele num: 10342
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16314
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66496
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.730702665282105e-4
allele num: 11556
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.448e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.64e-1

DP
type: SiteQuality
SIO_000300: 2.161472e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.3e-2

MQ
type: SiteQuality
SIO_000300: 5.938e1

VQSLOD
type: SiteQuality
SIO_000300: 5.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 4.454e0

QD
type: SiteQuality
SIO_000300: 1.272e1

MQRankSum
type: SiteQuality
SIO_000300: 8.86e-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: 4024
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GenotypeQuality
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GenotypeQuality
all individuals: 12716
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GenotypeQuality
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GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66476
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16244
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.53e-1

FS
type: SiteQuality
SIO_000300: 4.124e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.042e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.76e0

DP
type: SiteQuality
SIO_000300: 2.155357e6

GenotypeQuality
all individuals: 668
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2606
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 866
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 5
allele frequency: 4.329754069968826e-4
allele num: 11548
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.682416731216112e-5
allele num: 10328
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 29
allele frequency: 4.365234668994792e-4
allele num: 66434
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 6.789285273423034e-4
allele num: 16202
num of homozygotes: 1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.31e-2

FS
type: SiteQuality
SIO_000300: 9.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.3e0

DP
type: SiteQuality
SIO_000300: 2.146446e6

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

QD
type: SiteQuality
SIO_000300: 1.642e1

GenotypeQuality
all individuals: 22923
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2406
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4024
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4543
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4466
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66402
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: 16168
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 2.132e1

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.429e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.347e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.81e-1

FS
type: SiteQuality
SIO_000300: 1.521e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.34e0

MQ
type: SiteQuality
SIO_000300: 5.891e1

DP
type: SiteQuality
SIO_000300: 2.141578e6

GenotypeQuality
all individuals: 22922
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 74
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9110
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4024
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2406
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4542
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4464
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
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: 11538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16026
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66368
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.217e1

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 1.201e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

DP
type: SiteQuality
SIO_000300: 2.139248e6

GenotypeQuality
all individuals: 4461
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4543
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4024
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9184
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2405
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4617
bin: 6.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16028
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66368
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.667013347200555e-5
allele num: 11538
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: 6614
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 2.13918e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.18e-1

FS
type: SiteQuality
SIO_000300: 2.327e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.75e0

VQSLOD
type: SiteQuality
SIO_000300: 9.83e-1

QD
type: SiteQuality
SIO_000300: 1.489e1

GenotypeQuality
all individuals: 22924
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4460
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4540
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1048
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1109
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4025
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 2.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16008
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014772384684956e-5
allele num: 66340
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.139974e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.267e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e0

VQSLOD
type: SiteQuality
SIO_000300: 8.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.86e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.328e1

GenotypeQuality
all individuals: 2403
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4023
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4558
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4456
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4539
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

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