8-20022468-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022468
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022468
    reference: chr 8
allele count: 1
allele frequency: 8.270204108637402e-6
allele num: 120916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.927C>T
  hgvsp: ENST00000276373.5:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.927C>T
  hgvsp: ENST00000440926.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+90C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.927C>T
  hgvsp: ENST00000437980.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.927C>T
  hgvsp: ENST00000517776.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.927C>T
  hgvsp: ENST00000381608.4:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+90C>T
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9238
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29307
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5249
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3806
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile309Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

8-20022469-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022469
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022469
    reference: chr 8
allele count: 1
allele frequency: 8.269656974628692e-6
allele num: 120924
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.926T>A
  hgvsp: ENSP00000387549.1:p.Ile309Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.926T>A
  hgvsp: ENSP00000428001.1:p.Ile309Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.926T>A
  hgvsp: ENSP00000371021.4:p.Ile309Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+89T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.926T>A
  hgvsp: ENSP00000413361.1:p.Ile309Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+89T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.926T>A
  hgvsp: ENSP00000276373.5:p.Ile309Asn
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9241
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3465
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5249
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3806
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile309Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

8-20022470-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022470
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022470
    reference: chr 8
allele count: 1
allele frequency: 8.270067318347971e-6
allele num: 120918
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.925A>G
  hgvsp: ENSP00000371021.4:p.Ile309Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+88A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.925A>G
  hgvsp: ENSP00000387549.1:p.Ile309Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.925A>G
  hgvsp: ENSP00000276373.5:p.Ile309Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.925A>G
  hgvsp: ENSP00000428001.1:p.Ile309Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+88A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.925A>G
  hgvsp: ENSP00000413361.1:p.Ile309Val
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9802
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29381
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3806
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4736
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9244
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile309Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: T
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-20022472-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022472
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022472
    reference: chr 8
allele count: 20
allele frequency: 1.654095540558423e-4
allele num: 120912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+86C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.923C>T
  hgvsp: ENSP00000371021.4:p.Ser308Phe
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.923C>T
  hgvsp: ENSP00000413361.1:p.Ser308Phe
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.923C>T
  hgvsp: ENSP00000428001.1:p.Ser308Phe
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+86C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.923C>T
  hgvsp: ENSP00000276373.5:p.Ser308Phe
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.923C>T
  hgvsp: ENSP00000387549.1:p.Ser308Phe
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18823
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5269
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9242
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29261
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser308Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-20022473-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022473
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022473
    reference: chr 8
allele count: 1
allele frequency: 8.269930532583527e-6
allele num: 120920
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.922T>G
  hgvsp: ENSP00000428001.1:p.Ser308Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.922T>G
  hgvsp: ENSP00000387549.1:p.Ser308Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.922T>G
  hgvsp: ENSP00000413361.1:p.Ser308Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.922T>G
  hgvsp: ENSP00000276373.5:p.Ser308Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.922T>G
  hgvsp: ENSP00000371021.4:p.Ser308Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+85T>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+85T>G
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5255
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29332
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1876
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4729
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser308Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

8-20022478-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022478
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022478
    reference: chr 8
allele count: 2
allele frequency: 1.653767281868095e-5
allele num: 120936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.920-3C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+80C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.920-3C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.920-3C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.920-3C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.920-3C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+80C>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9842
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5263
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 29342
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3812
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
hgvs: c.920-3C>A
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

8-20022480-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022480
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022480
    reference: chr 8
allele count: 1
allele frequency: 8.26801600687899e-6
allele num: 120948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.920-5C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+78C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+78C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.920-5C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.920-5C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.920-5C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.920-5C>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3812
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
hgvs: c.920-5C>A
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

8-20022486-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022486
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022486
    reference: chr 8
allele count: 16188
allele frequency: 1.337563829259829e-1
allele num: 121026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+72A>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.920-11A>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.920-11A>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.920-11A>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.920-11A>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+72A>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.920-11A>T
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.75e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 5.75e1
  variant carriers: 1159
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 7.25e1
  variant carriers: 1296
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 4.25e1
  variant carriers: 595
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 6.25e1
  variant carriers: 1309
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 9.75e1
  variant carriers: 2022
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 5.25e1
  variant carriers: 939
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 9.25e1
  variant carriers: 677
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 1011
genotype depth: GenotypeDepth
  all individuals: 18255
  bin: 2.25e1
  variant carriers: 250
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.75e1
  variant carriers: 1239
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 3.75e1
  variant carriers: 502
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 15023
  bin: 2.75e1
  variant carriers: 362
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.75e1
  variant carriers: 1362
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 8.75e1
  variant carriers: 830
genotype depth: GenotypeDepth
  all individuals: 7610
  bin: 3.25e1
  variant carriers: 459
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.75e1
  variant carriers: 747
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 6995
  bin: 6.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2302
  bin: 8.25e1
  variant carriers: 13
num of homozygotes: 1273
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

8-20022486-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022486
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022486
    reference: chr 8
allele count: 11
allele frequency: 9.088956092079388e-5
allele num: 121026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.920-11A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.920-11A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.920-11A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+72A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+72A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.920-11A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.920-11A>G
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18255
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3320
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2302
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

8-20022487-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022487
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022487
    reference: chr 8
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.920-12C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.920-12C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.920-12C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+71C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+71C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.920-12C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.920-12C>G
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18724
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3610
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4706
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

8-20022489-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022489
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022489
    reference: chr 8
allele count: 2
allele frequency: 1.651636772041093e-5
allele num: 121092
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.920-14A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+69A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.920-14A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.920-14A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.920-14A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+69A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.920-14A>G
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1477
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3613
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3412
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28983
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-20022490-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022490
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022490
    reference: chr 8
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.920-15G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.920-15G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.920-15G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+68G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+68G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.920-15G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.920-15G>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4705
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS

8-20022495-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022495
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022495
    reference: chr 8
allele count: 1
allele frequency: 8.258865892535638e-6
allele num: 121082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.920-20T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.920-20T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+63T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+63T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.920-20T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.920-20T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.920-20T>C
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9064
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3614
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/8-20022498-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022498
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022498
    reference: chr 8
allele count: 2
allele frequency: 1.65169133192389e-5
allele num: 121088
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.920-23T>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.920-23T>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+60T>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.920-23T>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.920-23T>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.920-23T>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+60T>G
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18791
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28911
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3605
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4681
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

8-20022500-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022500
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022500
    reference: chr 8
allele count: 1
allele frequency: 8.260230295220631e-6
allele num: 121062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.920-25G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.920-25G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.920-25G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+58G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.920-25G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+58G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.920-25G>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4681
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP

8-20022501-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022501
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022501
    reference: chr 8
allele count: 274
allele frequency: 2.262891876713686e-3
allele num: 121084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+57G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.920-26G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.920-26G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.920-26G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.920-26G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.920-26G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+57G>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 5.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 18540
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 4.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 11167
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 18761
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28827
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3576
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 4
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-20022502-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022502
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022502
    reference: chr 8
allele count: 17
allele frequency: 1.403914443802131e-4
allele num: 121090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.920-27C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.920-27C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.920-27C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+56C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.920-27C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+56C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.920-27C>T
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18825
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11160
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9044
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4674
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3394
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD

8-20022508-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022508
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022508
    reference: chr 8
allele count: 1
allele frequency: 8.25559316436886e-6
allele num: 121130
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.920-33C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.920-33C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.920-33C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+50C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+50C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.920-33C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.920-33C>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6318
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1473
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4683
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29167
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD

8-20022513-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022513
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022513
    reference: chr 8
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.920-38T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.920-38T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.920-38T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+45T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+45T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.920-38T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.920-38T>C
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1941
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29319
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-20022527-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022527
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022527
    reference: chr 8
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.919+31G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.919+31G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.919+31G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+31G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+31G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.919+31G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.919+31G>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1942
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3408
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ

8-20022529-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022529
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022529
    reference: chr 8
allele count: 12
allele frequency: 9.898213372486267e-5
allele num: 121234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+29G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.919+29G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+29G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.919+29G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.919+29G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.919+29G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.919+29G>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6329
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3409
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1942
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

8-20022530-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022530
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022530
    reference: chr 8
allele count: 2
allele frequency: 1.649511744523621e-5
allele num: 121248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.919+28C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+28C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.919+28C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.919+28C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.919+28C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.919+28C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+28C>T
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29652
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3411
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1944
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4711
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-20022530-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022530
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022530
    reference: chr 8
allele count: 1
allele frequency: 8.247558722618106e-6
allele num: 121248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.919+28C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.919+28C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+28C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.919+28C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+28C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.919+28C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.919+28C>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29652
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6319
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ

8-20022537-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022537
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022537
    reference: chr 8
allele count: 2
allele frequency: 1.649212501030758e-5
allele num: 121270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+21C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+21C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.919+21C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.919+21C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.919+21C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.919+21C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.919+21C>T
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3412
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6317
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

8-20022541-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022541
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022541
    reference: chr 8
allele count: 282
allele frequency: 2.325351276469424e-3
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.919+17C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.919+17C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+17C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.919+17C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.919+17C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.919+17C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+17C>G
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.75e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 11286
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19298
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18628
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9176
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6351
  bin: 9.75e1
  variant carriers: 278
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 3
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

8-20022547-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022547
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022547
    reference: chr 8
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.919+11G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+11G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.919+11G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.919+11G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+11G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.919+11G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.919+11G>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3629
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9221
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3421
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-20022548-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022548
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022548
    reference: chr 8
allele count: 12
allele frequency: 9.894132779261898e-5
allele num: 121284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.919+10C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.919+10C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.919+10C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.919+10C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.919+10C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.919+10C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.919+10C>T
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11346
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19370
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29867
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4735
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6158
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 3632
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9221
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3420
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

8-20022563-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022563
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022563
    reference: chr 8
allele count: 2
allele frequency: 1.648641519388024e-5
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.914C>T
  hgvsp: ENSP00000387549.1:p.Ala305Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.914C>T
  hgvsp: ENSP00000429664.1:p.Ala305Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.914C>T
  hgvsp: ENSP00000276373.5:p.Ala305Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.914C>T
  hgvsp: ENSP00000371021.4:p.Ala305Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.914C>T
  hgvsp: ENSP00000413361.1:p.Ala305Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.914C>T
  hgvsp: ENSP00000428001.1:p.Ala305Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.914C>T
  hgvsp: ENSP00000265808.7:p.Ala305Val
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9210
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4735
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6150
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Ala305Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-20022574-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022574
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022574
    reference: chr 8
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.903C>A
  hgvsp: ENSP00000429664.1:p.Tyr301Ter
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.903C>A
  hgvsp: ENSP00000387549.1:p.Tyr301Ter
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.903C>A
  hgvsp: ENSP00000265808.7:p.Tyr301Ter
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.903C>A
  hgvsp: ENSP00000371021.4:p.Tyr301Ter
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.903C>A
  hgvsp: ENSP00000276373.5:p.Tyr301Ter
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.903C>A
  hgvsp: ENSP00000428001.1:p.Tyr301Ter
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.903C>A
  hgvsp: ENSP00000413361.1:p.Tyr301Ter
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29899
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3631
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr301Ter
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD

8-20022583-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022583
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022583
    reference: chr 8
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.894A>C
  hgvsp: ENSP00000265808.7:p.Lys298Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.894A>C
  hgvsp: ENSP00000429664.1:p.Lys298Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.894A>C
  hgvsp: ENSP00000276373.5:p.Lys298Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.894A>C
  hgvsp: ENSP00000371021.4:p.Lys298Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.894A>C
  hgvsp: ENSP00000428001.1:p.Lys298Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.894A>C
  hgvsp: ENSP00000413361.1:p.Lys298Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.894A>C
  hgvsp: ENSP00000387549.1:p.Lys298Asn
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9204
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4732
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys298Asn
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

8-20022585-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022585
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022585
    reference: chr 8
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.892A>G
  hgvsp: ENSP00000276373.5:p.Lys298Glu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.892A>G
  hgvsp: ENSP00000429664.1:p.Lys298Glu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.892A>G
  hgvsp: ENSP00000265808.7:p.Lys298Glu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.892A>G
  hgvsp: ENSP00000428001.1:p.Lys298Glu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.892A>G
  hgvsp: ENSP00000387549.1:p.Lys298Glu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.892A>G
  hgvsp: ENSP00000371021.4:p.Lys298Glu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.892A>G
  hgvsp: ENSP00000413361.1:p.Lys298Glu
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4731
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6149
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3422
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys298Glu
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-20022592-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022592
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022592
    reference: chr 8
allele count: 4
allele frequency: 3.299404457495422e-5
allele num: 121234
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.885G>A
  hgvsp: ENSP00000387549.1:p.Met295Ile
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.885G>A
  hgvsp: ENSP00000413361.1:p.Met295Ile
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.885G>A
  hgvsp: ENSP00000371021.4:p.Met295Ile
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.885G>A
  hgvsp: ENSP00000265808.7:p.Met295Ile
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.885G>A
  hgvsp: ENSP00000429664.1:p.Met295Ile
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.885G>A
  hgvsp: ENSP00000276373.5:p.Met295Ile
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.885G>A
  hgvsp: ENSP00000428001.1:p.Met295Ile
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6150
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3420
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1963
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4728
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9194
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Met295Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

8-20022594-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022594
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022594
    reference: chr 8
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.883A>G
  hgvsp: ENSP00000428001.1:p.Met295Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.883A>G
  hgvsp: ENSP00000387549.1:p.Met295Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.883A>G
  hgvsp: ENSP00000429664.1:p.Met295Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.883A>G
  hgvsp: ENSP00000265808.7:p.Met295Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.883A>G
  hgvsp: ENSP00000371021.4:p.Met295Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.883A>G
  hgvsp: ENSP00000413361.1:p.Met295Val
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.883A>G
  hgvsp: ENSP00000276373.5:p.Met295Val
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9192
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29813
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met295Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

8-20022595-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022595
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022595
    reference: chr 8
allele count: 2
allele frequency: 1.649919978881024e-5
allele num: 121218
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.882T>A
  hgvsp: ENSP00000265808.7:p.Phe294Leu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.882T>A
  hgvsp: ENSP00000276373.5:p.Phe294Leu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.882T>A
  hgvsp: ENSP00000413361.1:p.Phe294Leu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.882T>A
  hgvsp: ENSP00000387549.1:p.Phe294Leu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.882T>A
  hgvsp: ENSP00000371021.4:p.Phe294Leu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.882T>A
  hgvsp: ENSP00000429664.1:p.Phe294Leu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.882T>A
  hgvsp: ENSP00000428001.1:p.Phe294Leu
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6151
  bin: 9.75e1
  variant carriers: 2
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: 1483
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe294Leu
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

8-20022596-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022596
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022596
    reference: chr 8
allele count: 3
allele frequency: 2.474879968321537e-5
allele num: 121218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.881T>C
  hgvsp: ENSP00000371021.4:p.Phe294Ser
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.881T>C
  hgvsp: ENSP00000413361.1:p.Phe294Ser
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.881T>C
  hgvsp: ENSP00000428001.1:p.Phe294Ser
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.881T>C
  hgvsp: ENSP00000387549.1:p.Phe294Ser
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.881T>C
  hgvsp: ENSP00000265808.7:p.Phe294Ser
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.881T>C
  hgvsp: ENSP00000276373.5:p.Phe294Ser
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.881T>C
  hgvsp: ENSP00000429664.1:p.Phe294Ser
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9188
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3421
  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: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe294Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

8-20022598-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022598
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022598
    reference: chr 8
allele count: 3
allele frequency: 2.474920802534319e-5
allele num: 121216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.879C>G
  hgvsp: ENST00000437980.1:c.879C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.879C>G
  hgvsp: ENST00000519026.1:c.879C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.879C>G
  hgvsp: ENST00000440926.1:c.879C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.879C>G
  hgvsp: ENST00000265808.7:c.879C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.879C>G
  hgvsp: ENST00000381608.4:c.879C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.879C>G
  hgvsp: ENST00000276373.5:c.879C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.879C>G
  hgvsp: ENST00000517776.1:c.879C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4730
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1483
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu293Leu
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

8-20022603-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022603
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022603
    reference: chr 8
allele count: 2
allele frequency: 1.650818806127839e-5
allele num: 121152
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.874C>G
  hgvsp: ENSP00000429664.1:p.Pro292Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.874C>G
  hgvsp: ENSP00000387549.1:p.Pro292Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.874C>G
  hgvsp: ENSP00000371021.4:p.Pro292Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.874C>G
  hgvsp: ENSP00000265808.7:p.Pro292Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.874C>G
  hgvsp: ENSP00000276373.5:p.Pro292Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.874C>G
  hgvsp: ENSP00000428001.1:p.Pro292Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.874C>G
  hgvsp: ENSP00000413361.1:p.Pro292Ala
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4728
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9179
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro292Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

8-20022612-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022612
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022612
    reference: chr 8
allele count: 1
allele frequency: 8.257501940512956e-6
allele num: 121102
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.865A>G
  hgvsp: ENSP00000413361.1:p.Lys289Glu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.865A>G
  hgvsp: ENSP00000428001.1:p.Lys289Glu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.865A>G
  hgvsp: ENSP00000387549.1:p.Lys289Glu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.865A>G
  hgvsp: ENSP00000265808.7:p.Lys289Glu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.865A>G
  hgvsp: ENSP00000371021.4:p.Lys289Glu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.865A>G
  hgvsp: ENSP00000276373.5:p.Lys289Glu
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.865A>G
  hgvsp: ENSP00000429664.1:p.Lys289Glu
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3621
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6151
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29708
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys289Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

8-20022616-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022616
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022616
    reference: chr 8
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.861T>C
  hgvsp: ENST00000440926.1:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.861T>C
  hgvsp: ENST00000265808.7:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.861T>C
  hgvsp: ENST00000519026.1:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.861T>C
  hgvsp: ENST00000276373.5:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.861T>C
  hgvsp: ENST00000517776.1:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.861T>C
  hgvsp: ENST00000437980.1:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.861T>C
  hgvsp: ENST00000381608.4:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6152
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3619
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3416
  bin: 8.25e1
  variant carriers: 0
hgvs: c.861T>C
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

8-20022617-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022617
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022617
    reference: chr 8
allele count: 8
allele frequency: 6.608184236176505e-5
allele num: 121062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.860G>A
  hgvsp: ENSP00000428001.1:p.Ser287Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.860G>A
  hgvsp: ENSP00000371021.4:p.Ser287Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.860G>A
  hgvsp: ENSP00000387549.1:p.Ser287Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.860G>A
  hgvsp: ENSP00000265808.7:p.Ser287Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.860G>A
  hgvsp: ENSP00000276373.5:p.Ser287Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.860G>A
  hgvsp: ENSP00000413361.1:p.Ser287Asn
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.860G>A
  hgvsp: ENSP00000429664.1:p.Ser287Asn
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3619
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6156
  bin: 9.75e1
  variant carriers: 8
hgvs: p.Ser287Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum

8-20022625-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022625
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022625
    reference: chr 8
allele count: 1
allele frequency: 8.26801600687899e-6
allele num: 120948
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.859-7T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.859-7T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.859-7T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.859-7T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.859-7T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.859-7T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.859-7T>C
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9135
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29351
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6152
  bin: 9.75e1
  variant carriers: 1
hgvs: c.859-7T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

8-20022630-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022630
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022630
    reference: chr 8
allele count: 1
allele frequency: 8.270477702792114e-6
allele num: 120912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.859-12C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.859-12C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.859-12C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.859-12C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.859-12C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.859-12C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.859-12C>T
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11299
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1959
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9125
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-20022646-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022646
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022646
    reference: chr 8
allele count: 1
allele frequency: 8.286926544683108e-6
allele num: 120672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.859-28G>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.859-28G>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.859-28G>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.859-28G>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.859-28G>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.859-28G>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.859-28G>T
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3586
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27961
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1474
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1955
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ

8-20022647-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022647
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022647
    reference: chr 8
allele count: 2
allele frequency: 1.657193046417977e-5
allele num: 120686
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.859-29T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.859-29T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.859-29T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.859-29T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.859-29T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.859-29T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.859-29T>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18729
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27821
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3404
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1955
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6148
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3588
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

8-20022649-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022649
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022649
    reference: chr 8
allele count: 1
allele frequency: 8.288437629506838e-6
allele num: 120650
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.859-31A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.859-31A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.859-31A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.859-31A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.859-31A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.859-31A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.859-31A>C
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3403
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4685
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6147
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

8-20022651-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022651
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022651
    reference: chr 8
allele count: 1
allele frequency: 8.2917364554485e-6
allele num: 120602
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.859-33C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.859-33C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.859-33C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.859-33C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.859-33C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.859-33C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.859-33C>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1470
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4674
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1955
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

8-20022653-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022653
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022653
    reference: chr 8
allele count: 34
allele frequency: 2.819845074394148e-4
allele num: 120574
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.859-35T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.859-35T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.859-35T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.859-35T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.859-35T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.859-35T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.859-35T>C
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10675
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 16348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17798
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25261
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3399
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

8-20022656-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022656
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022656
    reference: chr 8
allele count: 1
allele frequency: 8.295450774795103e-6
allele num: 120548
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.859-38C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.859-38C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.859-38C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.859-38C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.859-38C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.859-38C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.859-38C>G
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1206
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3395
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3495
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

8-20022657-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022657
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022657
    reference: chr 8
allele count: 33
allele frequency: 2.737998440170586e-4
allele num: 120526
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.859-39A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.859-39A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.859-39A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.859-39A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.859-39A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.859-39A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.859-39A>C
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10425
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4775
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16093
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17336
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1449
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24077
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1466
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4617
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3486
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD

8-20022661-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022661
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022661
    reference: chr 8
allele count: 2
allele frequency: 1.660274609420398e-5
allele num: 120462
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.859-43A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.859-43A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.859-43A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.859-43A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.859-43A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.859-43A>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.859-43A>G
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4301
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1835
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8338
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4596
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3383
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1951
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3447
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS

8-20022664-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20022664
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20022664
    reference: chr 8
allele count: 1
allele frequency: 8.314763694415805e-6
allele num: 120268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.859-46T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.859-46T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.859-46T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.859-46T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.859-46T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.859-46T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.859-46T>C
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9901
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4738
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3427
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3375
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1642
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2457
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2219
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6142
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

8-20028566-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028566
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028567
    reference: chr 8
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.858+47dupG
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.858+47dupG
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.858+47dupG
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.858+47dupG
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.858+47dupG
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.858+47dupG
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.858+47dupG
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3890
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2361
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3895
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3613
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4162
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2532
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS

8-20028569-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028569
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028569
    reference: chr 8
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.858+45C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.858+45C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.858+45C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.858+45C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.858+45C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.858+45C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.858+45C>G
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8581
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3860
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3847
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2524
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4195
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

8-20028577-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028577
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028577
    reference: chr 8
allele count: 2
allele frequency: 1.649974425396406e-5
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.858+37C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.858+37C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.858+37C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.858+37C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.858+37C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.858+37C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.858+37C>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7257
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8373
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2515
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30744
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

8-20028579-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028579
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028579
    reference: chr 8
allele count: 3
allele frequency: 2.474349246148263e-5
allele num: 121244
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.858+35T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.858+35T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.858+35T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.858+35T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.858+35T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.858+35T>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.858+35T>C
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5811
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2362
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3620
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-20028583-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028583
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028583
    reference: chr 8
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.858+31G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.858+31G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.858+31G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.858+31G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.858+31G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.858+31G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.858+31G>C
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8971
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3860
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3874
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2518
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

8-20028589-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028589
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028589
    reference: chr 8
allele count: 3
allele frequency: 2.473492406378312e-5
allele num: 121286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.858+25C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.858+25C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.858+25C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.858+25C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.858+25C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.858+25C>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.858+25C>T
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3883
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9018
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3854
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3621
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

8-20028592-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028592
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028592
    reference: chr 8
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.858+22T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.858+22T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.858+22T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.858+22T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.858+22T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.858+22T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.858+22T>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5811
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3855
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30747
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3620
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

8-20028597-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028597
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028597
    reference: chr 8
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.858+17C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.858+17C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.858+17C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.858+17C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.858+17C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.858+17C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.858+17C>G
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7257
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4326
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30747
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3885
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9127
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/8-20028598-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028598
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028598
    reference: chr 8
allele count: 3
allele frequency: 2.47320692497939e-5
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.858+16G>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.858+16G>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.858+16G>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.858+16G>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.858+16G>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.858+16G>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.858+16G>T
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8602
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2538
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3857
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3886
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9123
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3620
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

8-20028598-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028598
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028598
    reference: chr 8
allele count: 4
allele frequency: 3.297609233305853e-5
allele num: 121300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.858+16G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.858+16G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.858+16G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.858+16G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.858+16G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.858+16G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.858+16G>C
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8602
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9123
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4324
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3886
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

8-20028606-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028606
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028606
    reference: chr 8
allele count: 2
allele frequency: 1.648505629646725e-5
allele num: 121322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.858+8G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.858+8G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.858+8G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.858+8G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.858+8G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.858+8G>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.858+8G>C
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3619
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2365
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4331
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
hgvs: c.858+8G>C
num of homozygotes: 1
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff

8-20028610-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028610
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028610
    reference: chr 8
allele count: 3
allele frequency: 2.472595400972554e-5
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.858+4A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.858+4A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.858+4A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.858+4A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.858+4A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.858+4A>C
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.858+4A>C
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5811
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30746
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3619
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2365
  bin: 8.75e1
  variant carriers: 0
hgvs: c.858+4A>C
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

8-20028613-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028613
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028613
    reference: chr 8
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.858+1G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.858+1G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.858+1G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.858+1G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.858+1G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.858+1G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.858+1G>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9248
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3619
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2366
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3861
  bin: 8.25e1
  variant carriers: 0
hgvs: c.858+1G>A
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-20028616-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028616
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028616
    reference: chr 8
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.856G>T
  hgvsp: ENSP00000276373.5:p.Glu286Ter
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.856G>T
  hgvsp: ENSP00000429664.1:p.Glu286Ter
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.856G>T
  hgvsp: ENSP00000413361.1:p.Glu286Ter
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428999
  ensembl transcript: ENST00000522513
  gene symbol: SLC18A1
  hgvsc: ENST00000522513.1:c.772G>T
  hgvsp: ENSP00000428999.1:p.Glu258Ter
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.856G>T
  hgvsp: ENSP00000371021.4:p.Glu286Ter
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.856G>T
  hgvsp: ENSP00000428001.1:p.Glu286Ter
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000036565
  ensembl transcript: ENST00000524272
  gene symbol: SLC18A1
  hgvsc: ENST00000524272.1:n.908G>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.856G>T
  hgvsp: ENSP00000387549.1:p.Glu286Ter
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.856G>T
  hgvsp: ENSP00000265808.7:p.Glu286Ter
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3877
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3862
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu286Ter
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

8-20028617-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028617
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028617
    reference: chr 8
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.855T>A
  hgvsp: ENST00000381608.4:c.855T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.855T>A
  hgvsp: ENST00000437980.1:c.855T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.855T>A
  hgvsp: ENST00000519026.1:c.855T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000036565
  ensembl transcript: ENST00000524272
  gene symbol: SLC18A1
  hgvsc: ENST00000524272.1:n.907T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.855T>A
  hgvsp: ENST00000276373.5:c.855T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.855T>A
  hgvsp: ENST00000440926.1:c.855T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.855T>A
  hgvsp: ENST00000265808.7:c.855T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428999
  ensembl transcript: ENST00000522513
  gene symbol: SLC18A1
  hgvsc: ENST00000522513.1:c.771T>A
  hgvsp: ENST00000522513.1:c.771T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.855T>A
  hgvsp: ENST00000517776.1:c.855T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9266
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro285Pro
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/8-20028625-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028625
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028625
    reference: chr 8
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428999
  ensembl transcript: ENST00000522513
  gene symbol: SLC18A1
  hgvsc: ENST00000522513.1:c.763G>T
  hgvsp: ENSP00000428999.1:p.Val255Phe
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.847G>T
  hgvsp: ENSP00000371021.4:p.Val283Phe
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.847G>T
  hgvsp: ENSP00000265808.7:p.Val283Phe
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.847G>T
  hgvsp: ENSP00000276373.5:p.Val283Phe
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.847G>T
  hgvsp: ENSP00000413361.1:p.Val283Phe
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.847G>T
  hgvsp: ENSP00000429664.1:p.Val283Phe
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.847G>T
  hgvsp: ENSP00000387549.1:p.Val283Phe
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000036565
  ensembl transcript: ENST00000524272
  gene symbol: SLC18A1
  hgvsc: ENST00000524272.1:n.899G>T
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.847G>T
  hgvsp: ENSP00000428001.1:p.Val283Phe
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30757
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4339
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val283Phe
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-20028625-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028625
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028625
    reference: chr 8
allele count: 56
allele frequency: 4.614598612324274e-4
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.847G>A
  hgvsp: ENSP00000387549.1:p.Val283Ile
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.847G>A
  hgvsp: ENSP00000371021.4:p.Val283Ile
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.847G>A
  hgvsp: ENSP00000429664.1:p.Val283Ile
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.847G>A
  hgvsp: ENSP00000413361.1:p.Val283Ile
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428999
  ensembl transcript: ENST00000522513
  gene symbol: SLC18A1
  hgvsc: ENST00000522513.1:c.763G>A
  hgvsp: ENSP00000428999.1:p.Val255Ile
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.847G>A
  hgvsp: ENSP00000276373.5:p.Val283Ile
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.847G>A
  hgvsp: ENSP00000428001.1:p.Val283Ile
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.847G>A
  hgvsp: ENSP00000265808.7:p.Val283Ile
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000036565
  ensembl transcript: ENST00000524272
  gene symbol: SLC18A1
  hgvsc: ENST00000524272.1:n.899G>A
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 8592
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2542
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3875
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val283Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-20028631-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028631
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028631
    reference: chr 8
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000036565
  ensembl transcript: ENST00000524272
  gene symbol: SLC18A1
  hgvsc: ENST00000524272.1:n.893T>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.841T>A
  hgvsp: ENSP00000413361.1:p.Ser281Thr
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.841T>A
  hgvsp: ENSP00000276373.5:p.Ser281Thr
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.841T>A
  hgvsp: ENSP00000265808.7:p.Ser281Thr
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.841T>A
  hgvsp: ENSP00000429664.1:p.Ser281Thr
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.841T>A
  hgvsp: ENSP00000387549.1:p.Ser281Thr
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428999
  ensembl transcript: ENST00000522513
  gene symbol: SLC18A1
  hgvsc: ENST00000522513.1:c.757T>A
  hgvsp: ENSP00000428999.1:p.Ser253Thr
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.841T>A
  hgvsp: ENSP00000428001.1:p.Ser281Thr
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.841T>A
  hgvsp: ENSP00000371021.4:p.Ser281Thr
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  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: 1.75e1
  variant carriers: 0
hgvs: p.Ser281Thr
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

8-20028634-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028634
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028634
    reference: chr 8
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.838C>G
  hgvsp: ENSP00000428001.1:p.Pro280Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000036565
  ensembl transcript: ENST00000524272
  gene symbol: SLC18A1
  hgvsc: ENST00000524272.1:n.890C>G
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.838C>G
  hgvsp: ENSP00000276373.5:p.Pro280Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.838C>G
  hgvsp: ENSP00000413361.1:p.Pro280Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.838C>G
  hgvsp: ENSP00000265808.7:p.Pro280Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.838C>G
  hgvsp: ENSP00000429664.1:p.Pro280Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.838C>G
  hgvsp: ENSP00000387549.1:p.Pro280Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428999
  ensembl transcript: ENST00000522513
  gene symbol: SLC18A1
  hgvsc: ENST00000522513.1:c.754C>G
  hgvsp: ENSP00000428999.1:p.Pro252Ala
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.838C>G
  hgvsp: ENSP00000371021.4:p.Pro280Ala
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2365
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro280Ala
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

8-20028634-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028634
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028634
    reference: chr 8
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.838C>A
  hgvsp: ENSP00000429664.1:p.Pro280Thr
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.838C>A
  hgvsp: ENSP00000428001.1:p.Pro280Thr
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000036565
  ensembl transcript: ENST00000524272
  gene symbol: SLC18A1
  hgvsc: ENST00000524272.1:n.890C>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428999
  ensembl transcript: ENST00000522513
  gene symbol: SLC18A1
  hgvsc: ENST00000522513.1:c.754C>A
  hgvsp: ENSP00000428999.1:p.Pro252Thr
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.838C>A
  hgvsp: ENSP00000387549.1:p.Pro280Thr
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.838C>A
  hgvsp: ENSP00000413361.1:p.Pro280Thr
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.838C>A
  hgvsp: ENSP00000276373.5:p.Pro280Thr
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.838C>A
  hgvsp: ENSP00000265808.7:p.Pro280Thr
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.838C>A
  hgvsp: ENSP00000371021.4:p.Pro280Thr
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7259
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3877
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro280Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

8-20028635-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20028635
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 20028635
    reference: chr 8
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000387549
  ensembl transcript: ENST00000440926
  gene symbol: SLC18A1
  hgvsc: ENST00000440926.1:c.837G>A
  hgvsp: ENST00000440926.1:c.837G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000265808
  ensembl transcript: ENST00000265808
  gene symbol: SLC18A1
  hgvsc: ENST00000265808.7:c.837G>A
  hgvsp: ENST00000265808.7:c.837G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000429664
  ensembl transcript: ENST00000519026
  gene symbol: SLC18A1
  hgvsc: ENST00000519026.1:c.837G>A
  hgvsp: ENST00000519026.1:c.837G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000371021
  ensembl transcript: ENST00000381608
  gene symbol: SLC18A1
  hgvsc: ENST00000381608.4:c.837G>A
  hgvsp: ENST00000381608.4:c.837G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428999
  ensembl transcript: ENST00000522513
  gene symbol: SLC18A1
  hgvsc: ENST00000522513.1:c.753G>A
  hgvsp: ENST00000522513.1:c.753G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000276373
  ensembl transcript: ENST00000276373
  gene symbol: SLC18A1
  hgvsc: ENST00000276373.5:c.837G>A
  hgvsp: ENST00000276373.5:c.837G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000036565
  ensembl transcript: ENST00000524272
  gene symbol: SLC18A1
  hgvsc: ENST00000524272.1:n.889G>A
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000413361
  ensembl transcript: ENST00000437980
  gene symbol: SLC18A1
  hgvsc: ENST00000437980.1:c.837G>A
  hgvsp: ENST00000437980.1:c.837G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000036565
  ensembl protein: ENSP00000428001
  ensembl transcript: ENST00000517776
  gene symbol: SLC18A1
  hgvsc: ENST00000517776.1:c.837G>A
  hgvsp: ENST00000517776.1:c.837G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10934
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9013
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln279Gln
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 183
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3463
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66502
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.139489194499017e-5
allele num: 16288
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
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: 6604
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.35e0

MQRankSum
type: SiteQuality
SIO_000300: 1.83e0

QD
type: SiteQuality
SIO_000300: 4.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

DP
type: SiteQuality
SIO_000300: 1.674163e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: -3.219e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 4736
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GenotypeQuality
all individuals: 166
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503714174009804e-5
allele num: 66502
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16294
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: 6606
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e0

VQSLOD
type: SiteQuality
SIO_000300: 7.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 5.872e0

MQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

DP
type: SiteQuality
SIO_000300: 1.674311e6

QD
type: SiteQuality
SIO_000300: 1.07e1

GenotypeQuality
all individuals: 358
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 3.25e1
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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variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66500
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.138735420503377e-5
allele num: 16290
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 9.69e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -9.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

FS
type: SiteQuality
SIO_000300: 9.366e0

VQSLOD
type: SiteQuality
SIO_000300: -1.141e0

DP
type: SiteQuality
SIO_000300: 1.674338e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

GenotypeQuality
all individuals: 177
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1559
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3805
bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 122
bin: 4.25e1
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 1874
bin: 9.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4730
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.503940323647958e-4
allele num: 66492
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.5241836484164e-4
allele num: 16292
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

FS
type: SiteQuality
SIO_000300: 5.24e-1

DP
type: SiteQuality
SIO_000300: 1.675371e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.319e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

QD
type: SiteQuality
SIO_000300: 1.292e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-1

GenotypeQuality
all individuals: 144
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3805
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variant carriers: 0

GenotypeQuality
all individuals: 9244
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 1561
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variant carriers: 0

GenotypeQuality
all individuals: 118
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variant carriers: 0

GenotypeQuality
all individuals: 175
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variant carriers: 0

GenotypeQuality
all individuals: 3469
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66498
num of homozygotes: 0

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16294
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

QD
type: SiteQuality
SIO_000300: 1.343e1

MQRankSum
type: SiteQuality
SIO_000300: -1.46e-1

DP
type: SiteQuality
SIO_000300: 1.675032e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.67e0

FS
type: SiteQuality
SIO_000300: 4.444e0

VQSLOD
type: SiteQuality
SIO_000300: 9.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.76e-1

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4744
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3482
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.25e1
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GenotypeQuality
all individuals: 1562
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
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GenotypeQuality
all individuals: 9250
bin: 6.75e1
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GenotypeQuality
all individuals: 186
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1878
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16302
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66504
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.12e-1

FS
type: SiteQuality
SIO_000300: 4.276e0

DP
type: SiteQuality
SIO_000300: 1.676612e6

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.92e-2

QD
type: SiteQuality
SIO_000300: 1.427e1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.718e0

GenotypeQuality
all individuals: 125
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29352
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3487
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GenotypeQuality
all individuals: 1881
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GenotypeQuality
all individuals: 9256
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GenotypeQuality
all individuals: 4754
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variant carriers: 0

GenotypeQuality
all individuals: 92
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GenotypeQuality
all individuals: 168
bin: 3.25e1
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GenotypeQuality
all individuals: 1562
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5264
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
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: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16308
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.024e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.72e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

QD
type: SiteQuality
SIO_000300: 1.212e1

DP
type: SiteQuality
SIO_000300: 1.677037e6

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.72e-1

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3320
bin: 7.75e1
variant carriers: 24

GenotypeQuality
all individuals: 129
bin: 4.75e1
variant carriers: 5

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 988
bin: 8.75e1
variant carriers: 18

GenotypeQuality
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bin: 9.75e1
variant carriers: 14788

GenotypeQuality
all individuals: 24009
bin: 6.25e1
variant carriers: 8

GenotypeQuality
all individuals: 2741
bin: 7.25e1
variant carriers: 12

GenotypeQuality
all individuals: 122
bin: 5.25e1
variant carriers: 11

GenotypeQuality
all individuals: 120
bin: 2.75e1
variant carriers: 1

Other
type: Population
allele count: 159
allele frequency: 1.762749445676275e-1
allele num: 902
num of homozygotes: 18

South Asian
type: Population
allele count: 1234
allele frequency: 7.542787286063569e-2
allele num: 16360
num of homozygotes: 62

European (Finnish)
type: Population
allele count: 409
allele frequency: 6.185722928009679e-2
allele num: 6612
num of homozygotes: 21

East Asian
type: Population
allele count: 1384
allele frequency: 1.601851851851852e-1
allele num: 8640
num of homozygotes: 129

European (Non-Finnish)
type: Population
allele count: 10522
allele frequency: 1.58106686701728e-1
allele num: 66550
num of homozygotes: 876

Latino
type: Population
allele count: 1642
allele frequency: 1.419432918395574e-1
allele num: 11568
num of homozygotes: 133

African
type: Population
allele count: 838
allele frequency: 8.062343659803733e-2
allele num: 10394
num of homozygotes: 34

VQSLOD
type: SiteQuality
SIO_000300: 6.39e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.291945e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.68e-2

QD
type: SiteQuality
SIO_000300: 1.649e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

GenotypeQuality
all individuals: 6995
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2741
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18085
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
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variant carriers: 0

GenotypeQuality
all individuals: 122
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variant carriers: 0

GenotypeQuality
all individuals: 24009
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1160
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 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: 8640
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.058302867038676e-3
allele num: 10394
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16360
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.649e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.75e-1

DP
type: SiteQuality
SIO_000300: 2.291945e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.68e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: 6.39e0

GenotypeQuality
all individuals: 3409
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 6174
bin: 9.75e1
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GenotypeQuality
all individuals: 1480
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GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 29000
bin: 6.25e1
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GenotypeQuality
all individuals: 1953
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GenotypeQuality
all individuals: 9100
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66574
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.949e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.66e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.479e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.67e-1

DP
type: SiteQuality
SIO_000300: 1.781661e6

GenotypeQuality
all individuals: 4710
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9110
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6176
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.110228522546743e-5
allele num: 16366
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501817198810561e-5
allele num: 66586
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.43e0

QD
type: SiteQuality
SIO_000300: 1.603e1

MQRankSum
type: SiteQuality
SIO_000300: 5.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.25e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

DP
type: SiteQuality
SIO_000300: 1.781772e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.66e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.11e-1

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6173
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variant carriers: 1

GenotypeQuality
all individuals: 167
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variant carriers: 0

GenotypeQuality
all individuals: 3610
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9098
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variant carriers: 0

GenotypeQuality
all individuals: 28877
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variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 3407
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66582
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.116207951070337e-5
allele num: 16350
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.781939e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.221e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.69e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.613e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.019e0

VQSLOD
type: SiteQuality
SIO_000300: -2.339e0

QD
type: SiteQuality
SIO_000300: 1.645e1

FS
type: SiteQuality
SIO_000300: 2.311e0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 185
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4696
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
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GenotypeQuality
all individuals: 3403
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6149
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28922
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
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: 16376
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66572
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.751e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

FS
type: SiteQuality
SIO_000300: 9.12e-1

DP
type: SiteQuality
SIO_000300: 1.781918e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.087e0

QD
type: SiteQuality
SIO_000300: 1.675e1

GenotypeQuality
all individuals: 9073
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1944
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3390
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6145
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 184
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.926040061633282e-4
allele num: 10384
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66576
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.351e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 1.782694e6

MQRankSum
type: SiteQuality
SIO_000300: 9.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQ
type: SiteQuality
SIO_000300: 5.962e1

FS
type: SiteQuality
SIO_000300: 1.0857e1

VQSLOD
type: SiteQuality
SIO_000300: -1.345e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.27e-1

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

GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9051
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3595
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28904
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 283
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variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6143
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502268425322237e-5
allele num: 66566
num of homozygotes: 0

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.344e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.128e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.875e0

VQSLOD
type: SiteQuality
SIO_000300: -2.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

FS
type: SiteQuality
SIO_000300: 9.84e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.233e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 1.78265e6

GenotypeQuality
all individuals: 176
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3385
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1931
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6352
bin: 9.75e1
variant carriers: 270

GenotypeQuality
all individuals: 4670
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9014
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004266057802079e-5
allele num: 66572
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

African
type: Population
allele count: 263
allele frequency: 2.532254958598113e-2
allele num: 10386
num of homozygotes: 4

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

Latino
type: Population
allele count: 8
allele frequency: 6.91323885240235e-4
allele num: 11572
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.979e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.77e-2

FS
type: SiteQuality
SIO_000300: 3.36e0

DP
type: SiteQuality
SIO_000300: 1.793721e6

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

QD
type: SiteQuality
SIO_000300: 1.471e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

GenotypeQuality
all individuals: 124
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3587
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1935
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variant carriers: 0

GenotypeQuality
all individuals: 6333
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 28829
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variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 13
allele frequency: 7.928763112954379e-4
allele num: 16396
num of homozygotes: 1

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.506534474988734e-5
allele num: 66570
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.41e-1

DP
type: SiteQuality
SIO_000300: 1.792345e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.49e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.495e1

GenotypeQuality
all individuals: 114
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3401
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1937
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GenotypeQuality
all individuals: 144
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 96
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GenotypeQuality
all individuals: 3597
bin: 7.25e1
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GenotypeQuality
all individuals: 9096
bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50177209106746e-5
allele num: 66588
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

QD
type: SiteQuality
SIO_000300: 1.469e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.079e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

FS
type: SiteQuality
SIO_000300: 2.029e0

DP
type: SiteQuality
SIO_000300: 1.792015e6

VQSLOD
type: SiteQuality
SIO_000300: 6.13e-1

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3409
bin: 8.25e1
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GenotypeQuality
all individuals: 91
bin: 2.75e1
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GenotypeQuality
all individuals: 130
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 3612
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variant carriers: 0

GenotypeQuality
all individuals: 107
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variant carriers: 0

GenotypeQuality
all individuals: 4687
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variant carriers: 0

GenotypeQuality
all individuals: 9118
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6321
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
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: 16440
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.99e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.697e0

QD
type: SiteQuality
SIO_000300: 1.237e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

DP
type: SiteQuality
SIO_000300: 1.7937e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -2.671e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

GenotypeQuality
all individuals: 1475
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4707
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 6325
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GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 29581
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variant carriers: 0

GenotypeQuality
all individuals: 134
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GenotypeQuality
all individuals: 9171
bin: 6.75e1
variant carriers: 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: 6612
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
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: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.797674e6

MQRankSum
type: SiteQuality
SIO_000300: -7.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.398e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.73e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4707
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29624
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9168
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.003842459173871e-5
allele num: 66624
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

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

Latino
type: Population
allele count: 7
allele frequency: 6.049083995852057e-4
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

FS
type: SiteQuality
SIO_000300: 5.27e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 2.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.918e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.77e-1

QD
type: SiteQuality
SIO_000300: 1.247e1

DP
type: SiteQuality
SIO_000300: 1.798598e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.25e-1

GenotypeQuality
all individuals: 9176
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3614
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6319
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001560811622043e-5
allele num: 66632
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: 3.66e-1

DP
type: SiteQuality
SIO_000300: 1.798368e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.49e-1

QD
type: SiteQuality
SIO_000300: 1.351e1

FS
type: SiteQuality
SIO_000300: 2.605e0

MQ
type: SiteQuality
SIO_000300: 5.992e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-1

GenotypeQuality
all individuals: 9176
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1944
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4711
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3411
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500780405811022e-5
allele num: 66632
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

FS
type: SiteQuality
SIO_000300: 2.605e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.66e-1

DP
type: SiteQuality
SIO_000300: 1.798368e6

QD
type: SiteQuality
SIO_000300: 1.351e1

MQ
type: SiteQuality
SIO_000300: 5.992e1

GenotypeQuality
all individuals: 29764
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4714
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9186
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variant carriers: 0

GenotypeQuality
all individuals: 1945
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3615
bin: 7.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000750187546887e-5
allele num: 66650
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.64e-1

FS
type: SiteQuality
SIO_000300: 5.9e-1

QD
type: SiteQuality
SIO_000300: 1.198e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.58e0

MQRankSum
type: SiteQuality
SIO_000300: 6.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.798862e6

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3404
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29762
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4710
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1479
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 7.25e1
variant carriers: 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: 16500
num of homozygotes: 0

African
type: Population
allele count: 272
allele frequency: 2.620423892100193e-2
allele num: 10380
num of homozygotes: 3

Latino
type: Population
allele count: 8
allele frequency: 6.912044237083118e-4
allele num: 11574
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.806324e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.35e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

QD
type: SiteQuality
SIO_000300: 1.29e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.221e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.31e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-2

FS
type: SiteQuality
SIO_000300: 5.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.84e0

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

GenotypeQuality
all individuals: 4731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6149
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variant carriers: 1

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29856
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 9.25e1
variant carriers: 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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
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: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.791547e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.419999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

QD
type: SiteQuality
SIO_000300: 1.076e1

FS
type: SiteQuality
SIO_000300: 1.282e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.25e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1960
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variant carriers: 0

GenotypeQuality
all individuals: 1485
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variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
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: 9
allele frequency: 8.673862760215882e-4
allele num: 10376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

DP
type: SiteQuality
SIO_000300: 1.792159e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.45e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

QD
type: SiteQuality
SIO_000300: 1.159e1

GenotypeQuality
all individuals: 3630
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1964
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variant carriers: 0

GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 29913
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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: 8
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variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999400119976005e-5
allele num: 66680
num of homozygotes: 0

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.791963e6

QD
type: SiteQuality
SIO_000300: 1.209e1

MQRankSum
type: SiteQuality
SIO_000300: 7.77e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.012e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

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

GenotypeQuality
all individuals: 9210
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variant carriers: 0

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

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 1962
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e-1

DP
type: SiteQuality
SIO_000300: 1.791684e6

FS
type: SiteQuality
SIO_000300: 1.006e0

QD
type: SiteQuality
SIO_000300: 1.099e1

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 29882
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
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GenotypeQuality
all individuals: 3629
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GenotypeQuality
all individuals: 10
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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: 9.25e1
variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

VQSLOD
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MQ
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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MQRankSum
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InbreedingCoeff
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QD
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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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South Asian
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66650
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Latino
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East Asian
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African
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
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DP
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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FS
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ReadPosRankSum
type: SiteQuality
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MQ
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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East Asian
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African
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South Asian
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Other
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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FS
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DP
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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MQ
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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variant carriers: 3

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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Other
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East Asian
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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DP
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MQ
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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Other
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FS
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VQSLOD
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MQRankSum
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MQ
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QD
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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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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Other
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FS
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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DP
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InbreedingCoeff
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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Other
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African
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European (Non-Finnish)
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South Asian
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MQ
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InbreedingCoeff
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VQSLOD
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QD
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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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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 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: 10338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66532
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.926e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.46e0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
SIO_000300: 2.217e0

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.652e0

DP
type: SiteQuality
SIO_000300: 1.787174e6

GenotypeQuality
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bin: 5.25e1
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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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.202356618973188e-4
allele num: 66536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 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: 10340
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.787582e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.66e-1

QD
type: SiteQuality
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VQSLOD
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BaseQRankSum
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SIO_000300: -3.201e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 3.364e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: 5.85e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504438092372499e-5
allele num: 66470
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
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: 11530
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.784104e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e0

QD
type: SiteQuality
SIO_000300: 1.218e1

VQSLOD
type: SiteQuality
SIO_000300: 2.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.37e-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
all individuals: 27
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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
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: 66446
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.516e0

QD
type: SiteQuality
SIO_000300: 1.167e1

FS
type: SiteQuality
SIO_000300: 1.1459e1

MQ
type: SiteQuality
SIO_000300: 5.914e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.105e0

DP
type: SiteQuality
SIO_000300: 1.783243e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-1

GenotypeQuality
all individuals: 4684
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variant carriers: 0

GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 472
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variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50793172085168e-5
allele num: 66316
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
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: 11508
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.767793e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.433e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 7.096e0

QD
type: SiteQuality
SIO_000300: 1.252e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 366
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4689
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 19
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 81
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GenotypeQuality
all individuals: 8985
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.015317814497648e-5
allele num: 66328
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 1.76547e6

FS
type: SiteQuality
SIO_000300: 6.056e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.302e1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508250128201261e-5
allele num: 66302
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

FS
type: SiteQuality
SIO_000300: 3.963e0

DP
type: SiteQuality
SIO_000300: 1.759442e6

QD
type: SiteQuality
SIO_000300: 1.256e1

MQRankSum
type: SiteQuality
SIO_000300: 1.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

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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bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508887346470713e-5
allele num: 66274
num of homozygotes: 0

Latino
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South Asian
type: Population
allele count: 0
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African
type: Population
allele count: 0
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VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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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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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
all individuals: 8537
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variant carriers: 0

GenotypeQuality
all individuals: 401
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GenotypeQuality
all individuals: 1090
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GenotypeQuality
all individuals: 6175
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 594
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GenotypeQuality
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GenotypeQuality
all individuals: 3500
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.026634382566586e-4
allele num: 6608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 1
allele frequency: 6.082725060827251e-5
allele num: 16440
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European (Non-Finnish)
type: Population
allele count: 31
allele frequency: 4.677974286231665e-4
allele num: 66268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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East Asian
type: Population
allele count: 0
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allele num: 8570
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InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.02e0

FS
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.742006e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

GenotypeQuality
all individuals: 25144
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
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Other
type: Population
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African
type: Population
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South Asian
type: Population
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allele frequency: 6.084205402774397e-5
allele num: 16436
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
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European (Finnish)
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allele count: 0
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.166e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.092e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8422
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1352
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6165
bin: 9.75e1
variant carriers: 33

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

Latino
type: Population
allele count: 5
allele frequency: 4.347826086956522e-4
allele num: 11500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 27
allele frequency: 4.076579297016548e-4
allele num: 66232
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.725734292939116e-5
allele num: 10282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.731198e6

VQSLOD
type: SiteQuality
SIO_000300: 5.94e0

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.482e1

GenotypeQuality
all individuals: 77
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22808
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1298
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1516
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6142
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.021421881137263e-5
allele num: 66194
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: 11486
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 1.721763e6

QD
type: SiteQuality
SIO_000300: 1.271e1

MQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.19e0

FS
type: SiteQuality
SIO_000300: 5.755e0

GenotypeQuality
all individuals: 87
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19888
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1464
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8143
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4570
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 1.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513500423780119e-5
allele num: 66072
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.215e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-1

QD
type: SiteQuality
SIO_000300: 2.279e1

DP
type: SiteQuality
SIO_000300: 1.713168e6

GenotypeQuality
all individuals: 346
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6944
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variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30757
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501366243281386e-5
allele num: 66606
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.021e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.94e0

DP
type: SiteQuality
SIO_000300: 2.685109e6

MQRankSum
type: SiteQuality
SIO_000300: -2.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

QD
type: SiteQuality
SIO_000300: 1.179e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2353
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30741
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3608
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7443
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variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66608
num of homozygotes: 0

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.212e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.57e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

QD
type: SiteQuality
SIO_000300: 1.574e1

FS
type: SiteQuality
SIO_000300: 6.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-3

DP
type: SiteQuality
SIO_000300: 2.688087e6

VQSLOD
type: SiteQuality
SIO_000300: 9.99e-1

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 173
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3878
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3852
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3615
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 4252
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8404
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.457e0

FS
type: SiteQuality
SIO_000300: 7.68e-1

DP
type: SiteQuality
SIO_000300: 2.695254e6

VQSLOD
type: SiteQuality
SIO_000300: 4.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.44e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.15e-1

QD
type: SiteQuality
SIO_000300: 1.006e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2518
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8547
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3882
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30746
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4275
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3855
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.468208092485549e-4
allele num: 8650
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: 6608
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.522e1

DP
type: SiteQuality
SIO_000300: 2.696324e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.22e0

FS
type: SiteQuality
SIO_000300: 4.891e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.8e-2

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3618
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2363
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4281
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8760
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30745
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 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: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.631e0

QD
type: SiteQuality
SIO_000300: 1.769e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

DP
type: SiteQuality
SIO_000300: 2.6987e6

VQSLOD
type: SiteQuality
SIO_000300: -2.008e0

MQRankSum
type: SiteQuality
SIO_000300: -1.488e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.366e0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 4295
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variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30746
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2365
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.25e1
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: 10406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.467406380027739e-4
allele num: 8652
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.982e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.74e-1

FS
type: SiteQuality
SIO_000300: 2.896e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.115e0

DP
type: SiteQuality
SIO_000300: 2.700656e6

QD
type: SiteQuality
SIO_000300: 1.42e1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

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

GenotypeQuality
all individuals: 3888
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variant carriers: 0

GenotypeQuality
all individuals: 9084
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 61
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GenotypeQuality
all individuals: 4303
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variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

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

GenotypeQuality
all individuals: 2364
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

Other
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 1.2e-3

BaseQRankSum
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SIO_000300: -2.826e0

FS
type: SiteQuality
SIO_000300: 1.2058e1

MQ
type: SiteQuality
SIO_000300: 5.983e1

MQRankSum
type: SiteQuality
SIO_000300: -5.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.22e-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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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 9.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: -1.872e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.553e0

DP
type: SiteQuality
SIO_000300: 2.701785e6

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.84e-1

QD
type: SiteQuality
SIO_000300: 1.068e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66648
num of homozygotes: 0

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

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

Latino
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allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -7.77e-1

FS
type: SiteQuality
SIO_000300: 5.387e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.953e1

VQSLOD
type: SiteQuality
SIO_000300: 9.3e-1

DP
type: SiteQuality
SIO_000300: 2.702268e6

QD
type: SiteQuality
SIO_000300: 1.146e1

GenotypeQuality
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variant carriers: 4

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 904
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
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.001680470531749e-5
allele num: 66648
num of homozygotes: 0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.387e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.77e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

VQSLOD
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DP
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SIO_000300: 2.702268e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.81e-1

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
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bin: 9.75e1
variant carriers: 1

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.000120004800192e-5
allele num: 66664
num of homozygotes: 1

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 2.702869e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.499910001799964e-5
allele num: 66668
num of homozygotes: 0

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

Other
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.096e0

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

South Asian
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allele num: 16510
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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FS
type: SiteQuality
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DP
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MQRankSum
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QD
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MQ
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ClippingRankSum
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
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allele num: 16510
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

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

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

East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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allele frequency: 6.056935190793458e-5
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European (Non-Finnish)
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
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DP
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 3.6e-3

BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

Other
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MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

FS
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VQSLOD
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InbreedingCoeff
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SIO_000300: -4.0e-4

QD
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MQ
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.705911e6

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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