8-26628071-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628071
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628071
    reference: chr 8
allele count: 19
allele frequency: 1.565848030328004e-4
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.996G>A
  hgvsp: ENST00000380573.3:c.996G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.996G>A
  hgvsp: ENST00000380586.1:c.996G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13775G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.209G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21806G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21806G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.996G>A
  hgvsp: ENST00000519229.1:c.996G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.996G>A
  hgvsp: ENST00000276393.4:c.996G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.996G>A
  hgvsp: ENST00000380582.3:c.996G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.996G>A
  hgvsp: ENST00000354550.4:c.996G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13775G>A
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15216
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu332Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

8-26628073-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628073
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628073
    reference: chr 8
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21808G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.994G>A
  hgvsp: ENSP00000276393.4:p.Glu332Lys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.994G>A
  hgvsp: ENSP00000346557.4:p.Glu332Lys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.994G>A
  hgvsp: ENSP00000369956.3:p.Glu332Lys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.994G>A
  hgvsp: ENSP00000369960.1:p.Glu332Lys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21808G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13777G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.994G>A
  hgvsp: ENSP00000430793.1:p.Glu332Lys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13777G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.994G>A
  hgvsp: ENSP00000369947.3:p.Glu332Lys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.207G>A
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3357
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu332Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

8-26628075-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628075
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628075
    reference: chr 8
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.992A>T
  hgvsp: ENSP00000276393.4:p.Gln331Leu
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13779A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.992A>T
  hgvsp: ENSP00000346557.4:p.Gln331Leu
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21810A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.992A>T
  hgvsp: ENSP00000369956.3:p.Gln331Leu
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.992A>T
  hgvsp: ENSP00000369960.1:p.Gln331Leu
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.992A>T
  hgvsp: ENSP00000430793.1:p.Gln331Leu
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.205A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21810A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13779A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.992A>T
  hgvsp: ENSP00000369947.3:p.Gln331Leu
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln331Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-26628082-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628082
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628082
    reference: chr 8
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.198T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21817T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.985T>G
  hgvsp: ENSP00000369947.3:p.Ser329Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13786T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.985T>G
  hgvsp: ENSP00000276393.4:p.Ser329Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.985T>G
  hgvsp: ENSP00000369956.3:p.Ser329Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.985T>G
  hgvsp: ENSP00000369960.1:p.Ser329Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.985T>G
  hgvsp: ENSP00000430793.1:p.Ser329Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21817T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13786T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.985T>G
  hgvsp: ENSP00000346557.4:p.Ser329Ala
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser329Ala
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: A
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

8-26628089-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628089
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628089
    reference: chr 8
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.978C>T
  hgvsp: ENST00000354550.4:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.978C>T
  hgvsp: ENST00000519229.1:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.978C>T
  hgvsp: ENST00000380586.1:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21824C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.978C>T
  hgvsp: ENST00000276393.4:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.191C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.978C>T
  hgvsp: ENST00000380582.3:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21824C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13793C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.978C>T
  hgvsp: ENST00000380573.3:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13793C>T
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr326Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

8-26628095-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628095
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628095
    reference: chr 8
allele count: 3
allele frequency: 2.475778632379884e-5
allele num: 121174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.972C>A
  hgvsp: ENST00000276393.4:c.972C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.972C>A
  hgvsp: ENST00000354550.4:c.972C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13799C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21830C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.185C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13799C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.972C>A
  hgvsp: ENST00000380586.1:c.972C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.972C>A
  hgvsp: ENST00000519229.1:c.972C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.972C>A
  hgvsp: ENST00000380582.3:c.972C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.972C>A
  hgvsp: ENST00000380573.3:c.972C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21830C>A
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 30267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile324Ile
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-26628106-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628106
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628106
    reference: chr 8
allele count: 1
allele frequency: 8.258865892535638e-6
allele num: 121082
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.961A>G
  hgvsp: ENSP00000369960.1:p.Ile321Val
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.174A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13810A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21841A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.961A>G
  hgvsp: ENSP00000369947.3:p.Ile321Val
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13810A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.961A>G
  hgvsp: ENSP00000276393.4:p.Ile321Val
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.961A>G
  hgvsp: ENSP00000369956.3:p.Ile321Val
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21841A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.961A>G
  hgvsp: ENSP00000430793.1:p.Ile321Val
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.961A>G
  hgvsp: ENSP00000346557.4:p.Ile321Val
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile321Val
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

8-26628118-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628118
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628118
    reference: chr 8
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13822C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.949C>A
  hgvsp: ENSP00000369947.3:p.Leu317Ile
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21853C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.949C>A
  hgvsp: ENSP00000369956.3:p.Leu317Ile
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21853C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.949C>A
  hgvsp: ENSP00000276393.4:p.Leu317Ile
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.949C>A
  hgvsp: ENSP00000369960.1:p.Leu317Ile
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.949C>A
  hgvsp: ENSP00000346557.4:p.Leu317Ile
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13822C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.949C>A
  hgvsp: ENSP00000430793.1:p.Leu317Ile
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.162C>A
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8221
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu317Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

8-26628120-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628120
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628120
    reference: chr 8
allele count: 1
allele frequency: 8.28775070445881e-6
allele num: 120660
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21855A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.947A>G
  hgvsp: ENSP00000430793.1:p.Tyr316Cys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21855A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.947A>G
  hgvsp: ENSP00000346557.4:p.Tyr316Cys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.947A>G
  hgvsp: ENSP00000369960.1:p.Tyr316Cys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.947A>G
  hgvsp: ENSP00000369956.3:p.Tyr316Cys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.160A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.947A>G
  hgvsp: ENSP00000276393.4:p.Tyr316Cys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.947A>G
  hgvsp: ENSP00000369947.3:p.Tyr316Cys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13824A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13824A>G
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr316Cys
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

8-26628124-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628124
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628124
    reference: chr 8
allele count: 8
allele frequency: 6.637571976171117e-5
allele num: 120526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.943G>A
  hgvsp: ENSP00000276393.4:p.Gly315Arg
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.943G>A
  hgvsp: ENSP00000346557.4:p.Gly315Arg
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21859G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.943G>A
  hgvsp: ENSP00000369960.1:p.Gly315Arg
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.943G>A
  hgvsp: ENSP00000430793.1:p.Gly315Arg
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.943G>A
  hgvsp: ENSP00000369956.3:p.Gly315Arg
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13828G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.156G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.943G>A
  hgvsp: ENSP00000369947.3:p.Gly315Arg
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13828G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21859G>A
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly315Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

8-26628125-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628125
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628125
    reference: chr 8
allele count: 2
allele frequency: 1.660605456749531e-5
allele num: 120438
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.942C>T
  hgvsp: ENST00000380586.1:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.942C>T
  hgvsp: ENST00000519229.1:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13829C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.942C>T
  hgvsp: ENST00000380573.3:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.942C>T
  hgvsp: ENST00000354550.4:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.155C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21860C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.942C>T
  hgvsp: ENST00000276393.4:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.942C>T
  hgvsp: ENST00000380582.3:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21860C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13829C>T
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu314Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS

8-26628128-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628128
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628128
    reference: chr 8
allele count: 1
allele frequency: 8.310755780130645e-6
allele num: 120326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21863G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.939G>A
  hgvsp: ENSP00000276393.4:p.Trp313Ter
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13832G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.939G>A
  hgvsp: ENSP00000369956.3:p.Trp313Ter
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.939G>A
  hgvsp: ENSP00000369960.1:p.Trp313Ter
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.939G>A
  hgvsp: ENSP00000369947.3:p.Trp313Ter
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.939G>A
  hgvsp: ENSP00000346557.4:p.Trp313Ter
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.939G>A
  hgvsp: ENSP00000430793.1:p.Trp313Ter
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21863G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13832G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.152G>A
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Trp313Ter
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

8-26628135-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628135
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628135
    reference: chr 8
allele count: 1
allele frequency: 8.327642777435419e-6
allele num: 120082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.932T>C
  hgvsp: ENSP00000430793.1:p.Val311Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13839T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.932T>C
  hgvsp: ENSP00000346557.4:p.Val311Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.932T>C
  hgvsp: ENSP00000276393.4:p.Val311Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21870T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21870T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.145T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.932T>C
  hgvsp: ENSP00000369947.3:p.Val311Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13839T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.932T>C
  hgvsp: ENSP00000369956.3:p.Val311Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.932T>C
  hgvsp: ENSP00000369960.1:p.Val311Ala
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val311Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

8-26628140-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628140
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628140
    reference: chr 8
allele count: 1
allele frequency: 8.338336335134414e-6
allele num: 119928
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.927A>G
  hgvsp: ENST00000354550.4:c.927A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.927A>G
  hgvsp: ENST00000276393.4:c.927A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.927A>G
  hgvsp: ENST00000380573.3:c.927A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.140A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.927A>G
  hgvsp: ENST00000380586.1:c.927A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21875A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13844A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.927A>G
  hgvsp: ENST00000519229.1:c.927A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.927A>G
  hgvsp: ENST00000380582.3:c.927A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21875A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13844A>G
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29741
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8156
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys309Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

8-26628148-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628148
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628148
    reference: chr 8
allele count: 1
allele frequency: 8.370722560771445e-6
allele num: 119464
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.919G>A
  hgvsp: ENSP00000369956.3:p.Val307Ile
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13852G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.919G>A
  hgvsp: ENSP00000346557.4:p.Val307Ile
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21883G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.919G>A
  hgvsp: ENSP00000430793.1:p.Val307Ile
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.919G>A
  hgvsp: ENSP00000276393.4:p.Val307Ile
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.132G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21883G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.919G>A
  hgvsp: ENSP00000369947.3:p.Val307Ile
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.919G>A
  hgvsp: ENSP00000369960.1:p.Val307Ile
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13852G>A
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val307Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

8-26628149-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628149
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628149
    reference: chr 8
allele count: 1
allele frequency: 8.375209380234507e-6
allele num: 119400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.918A>G
  hgvsp: ENST00000519229.1:c.918A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.918A>G
  hgvsp: ENST00000276393.4:c.918A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13853A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21884A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21884A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.918A>G
  hgvsp: ENST00000354550.4:c.918A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.918A>G
  hgvsp: ENST00000380582.3:c.918A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.918A>G
  hgvsp: ENST00000380573.3:c.918A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.918A>G
  hgvsp: ENST00000380586.1:c.918A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13853A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.131A>G
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr306Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

8-26628152-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628152
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628152
    reference: chr 8
allele count: 1
allele frequency: 8.404915194405689e-6
allele num: 118978
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21887A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.915A>C
  hgvsp: ENSP00000369960.1:p.Glu305Asp
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.915A>C
  hgvsp: ENSP00000276393.4:p.Glu305Asp
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.128A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21887A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.915A>C
  hgvsp: ENSP00000369947.3:p.Glu305Asp
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.915A>C
  hgvsp: ENSP00000430793.1:p.Glu305Asp
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13856A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.915A>C
  hgvsp: ENSP00000369956.3:p.Glu305Asp
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.915A>C
  hgvsp: ENSP00000346557.4:p.Glu305Asp
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13856A>C
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu305Asp
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

8-26628155-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628155
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628155
    reference: chr 8
allele count: 1
allele frequency: 8.415949908266146e-6
allele num: 118822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.912T>A
  hgvsp: ENST00000519229.1:c.912T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21890T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.912T>A
  hgvsp: ENST00000354550.4:c.912T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.912T>A
  hgvsp: ENST00000380582.3:c.912T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13859T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.912T>A
  hgvsp: ENST00000276393.4:c.912T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.912T>A
  hgvsp: ENST00000380586.1:c.912T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.125T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13859T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21890T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.912T>A
  hgvsp: ENST00000380573.3:c.912T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser304Ser
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

8-26628161-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628161
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628161
    reference: chr 8
allele count: 3
allele frequency: 2.534854245880862e-5
allele num: 118350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.906G>A
  hgvsp: ENST00000276393.4:c.906G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21896G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.906G>A
  hgvsp: ENST00000380586.1:c.906G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.906G>A
  hgvsp: ENST00000380573.3:c.906G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.906G>A
  hgvsp: ENST00000354550.4:c.906G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21896G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.906G>A
  hgvsp: ENST00000380582.3:c.906G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.906G>A
  hgvsp: ENST00000519229.1:c.906G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13865G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13865G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.119G>A
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys302Lys
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

8-26628169-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628169
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628169
    reference: chr 8
allele count: 1
allele frequency: 8.512521919743944e-6
allele num: 117474
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.898G>A
  hgvsp: ENSP00000369956.3:p.Asp300Asn
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.111G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.898G>A
  hgvsp: ENSP00000430793.1:p.Asp300Asn
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.898G>A
  hgvsp: ENSP00000346557.4:p.Asp300Asn
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13873G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.898G>A
  hgvsp: ENSP00000276393.4:p.Asp300Asn
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.898G>A
  hgvsp: ENSP00000369960.1:p.Asp300Asn
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21904G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13873G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.898G>A
  hgvsp: ENSP00000369947.3:p.Asp300Asn
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21904G>A
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp300Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-26628172-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628172
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628172
    reference: chr 8
allele count: 1
allele frequency: 8.538105565137207e-6
allele num: 117122
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.895C>G
  hgvsp: ENSP00000369947.3:p.Pro299Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13876C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.895C>G
  hgvsp: ENSP00000369956.3:p.Pro299Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13876C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.895C>G
  hgvsp: ENSP00000430793.1:p.Pro299Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21907C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.895C>G
  hgvsp: ENSP00000346557.4:p.Pro299Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.895C>G
  hgvsp: ENSP00000369960.1:p.Pro299Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21907C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.895C>G
  hgvsp: ENSP00000276393.4:p.Pro299Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.108C>G
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro299Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-26628183-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628183
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628183
    reference: chr 8
allele count: 1
allele frequency: 8.686436997272459e-6
allele num: 115122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884G>T
  hgvsp: ENSP00000369956.3:p.Gly295Val
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884G>T
  hgvsp: ENSP00000369947.3:p.Gly295Val
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884G>T
  hgvsp: ENSP00000430793.1:p.Gly295Val
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13887G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884G>T
  hgvsp: ENSP00000276393.4:p.Gly295Val
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21918G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21918G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884G>T
  hgvsp: ENSP00000369960.1:p.Gly295Val
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884G>T
  hgvsp: ENSP00000346557.4:p.Gly295Val
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13887G>T
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26982
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly295Val
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

8-26628187-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628187
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628187
    reference: chr 8
allele count: 12
allele frequency: 1.049116119669179e-4
allele num: 114382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-4C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-4C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-4C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-4C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-4C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-4C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-4C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21922C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13891C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13891C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21922C>G
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26545
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13248
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.884-4C>G
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

8-26628207-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628207
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628207
    reference: chr 8
allele count: 2
allele frequency: 1.822622389093428e-5
allele num: 109732
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-24A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-24A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-24A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-24A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13911A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-24A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-24A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21942A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-24A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13911A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21942A>G
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21659
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD

8-26628208-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628208
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628208
    reference: chr 8
allele count: 1
allele frequency: 9.111617312072893e-6
allele num: 109750
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-25T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21943T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-25T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21943T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13912T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-25T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-25T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-25T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-25T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-25T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13912T>C
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8920
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9559
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2058
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

8-26628209-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628209
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628209
    reference: chr 8
allele count: 1
allele frequency: 9.147959090326949e-6
allele num: 109314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-26G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21944G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-26G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-26G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-26G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-26G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13913G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21944G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-26G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-26G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13913G>C
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9326
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/8-26628210-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628210
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628210
    reference: chr 8
allele count: 2
allele frequency: 1.832777390858107e-5
allele num: 109124
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13914T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21945T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-27T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-27T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-27T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-27T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13914T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-27T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-27T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-27T>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21945T>G
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20070
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9920
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8939
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1932
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

8-26628212-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628212
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628212
    reference: chr 8
allele count: 1
allele frequency: 9.196755384700277e-6
allele num: 108734
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-29T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21947T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-29T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13916T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-29T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-29T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21947T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13916T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-29T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-29T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-29T>C
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8486
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

8-26628224-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628224
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628224
    reference: chr 8
allele count: 1
allele frequency: 9.49920206702637e-6
allele num: 105272
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-41G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-41G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21959G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-41G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-41G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-41G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13928G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21959G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13928G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-41G>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-41G>C
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4828
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13840
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1463
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-26628230-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628230
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628229
    reference: chr 8
allele count: 1
allele frequency: 9.591774094536525e-6
allele num: 104256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13935delC
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-48delC
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-48delC
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21966delC
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-48delC
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-48delC
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21966delC
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-48delC
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13935delC
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-48delC
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-48delC
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10091
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: AG
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

8-26628235-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26628235
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26628235
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 102568
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-52T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-21970T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-52T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-13939T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-52T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-52T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-13939T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-21970T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-52T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-52T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-52T>C
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13418
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9982
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2496
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/8-26636769-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636769
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636769
    reference: chr 8
allele count: 1
allele frequency: 7.984669434685404e-5
allele num: 12524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.*33G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22473G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8586G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8586G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8586G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22473G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30504G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8586G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8586G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8586G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30504G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8586G>T
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

8-26636773-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636773
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636774
    reference: chr 8
allele count: 111
allele frequency: 9.748814333391885e-3
allele num: 11386
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8591dupA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8591dupA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22478dupA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8591dupA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8591dupA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8591dupA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8591dupA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30509dupA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22478dupA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.*28dupA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8591dupA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30509dupA
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 2.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 2.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 1.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

8-26636773-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636773
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636772
    reference: chr 8
allele count: 21
allele frequency: 1.844370279290357e-3
allele num: 11386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8591delA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22478delA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8591delA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8591delA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30509delA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8591delA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8591delA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22478delA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8591delA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.*28delA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8591delA
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30509delA
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 2.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: CT
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/8-26636794-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636794
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636794
    reference: chr 8
allele count: 1
allele frequency: 7.248477819657872e-5
allele num: 13796
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8611G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8611G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8611G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.*8G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8611G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22498G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30529G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8611G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8611G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30529G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22498G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8611G>T
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/8-26636798-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636798
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636798
    reference: chr 8
allele count: 2
allele frequency: 1.432664756446991e-4
allele num: 13960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8615G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22502G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.*4G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30533G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8615G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22502G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8615G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30533G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8615G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8615G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8615G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8615G>T
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

8-26636833-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636833
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636833
    reference: chr 8
allele count: 1
allele frequency: 7.048209754722301e-5
allele num: 14188
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.998T>C
  hgvsp: ENSP00000369946.3:p.Val333Ala
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8650T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8650T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8650T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30568T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8650T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8650T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30568T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8650T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22537T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22537T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8650T>C
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val333Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

8-26636882-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636882
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636882
    reference: chr 8
allele count: 15
allele frequency: 1.056338028169014e-3
allele num: 14200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.949G>A
  hgvsp: ENSP00000369946.3:p.Ala317Thr
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8699G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8699G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8699G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30617G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8699G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8699G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8699G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30617G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22586G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8699G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22586G>A
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala317Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

8-26636893-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636893
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636893
    reference: chr 8
allele count: 1
allele frequency: 7.057163020465773e-5
allele num: 14170
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30628C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8710C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8710C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8710C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8710C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22597C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8710C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.938C>G
  hgvsp: ENSP00000369946.3:p.Pro313Arg
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30628C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8710C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22597C>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8710C>G
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro313Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP

8-26636897-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636897
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636897
    reference: chr 8
allele count: 5
allele frequency: 3.532071206555524e-4
allele num: 14156
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8714C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8714C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.934C>T
  hgvsp: ENSP00000369946.3:p.Gln312Ter
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8714C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30632C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8714C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22601C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8714C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30632C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22601C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8714C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8714C>T
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln312Ter
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-26636898-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636898
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636898
    reference: chr 8
allele count: 5
allele frequency: 3.532570298148933e-4
allele num: 14154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8715A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8715A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8715A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8715A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30633A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22602A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.933A>G
  hgvsp: ENST00000380572.3:c.933A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22602A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8715A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8715A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30633A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8715A>G
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys311Lys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

8-26636906-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636906
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636906
    reference: chr 8
allele count: 2487
allele frequency: 1.759088980053756e-1
allele num: 14138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8723A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22610A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8723A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.925A>T
  hgvsp: ENSP00000369946.3:p.Ser309Cys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8723A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8723A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8723A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22610A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30641A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8723A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8723A>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30641A>T
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 2.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.75e1
  variant carriers: 255
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 168
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 2.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 196
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 2.5e0
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.25e1
  variant carriers: 161
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.25e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 168
genotype quality: GenotypeQuality
hgvs: p.Ser309Cys
num of homozygotes: 251
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

8-26636918-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636918
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636918
    reference: chr 8
allele count: 113
allele frequency: 8.057615516257844e-3
allele num: 14024
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8735A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8735A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8735A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22622A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8735A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.913A>G
  hgvsp: ENSP00000369946.3:p.Asn305Asp
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8735A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30653A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22622A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8735A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8735A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30653A>G
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 2.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Asn305Asp
num of homozygotes: 4
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-26636925-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636925
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636925
    reference: chr 8
allele count: 7298
allele frequency: 5.241309968399885e-1
allele num: 13924
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8742A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8742A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8742A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8742A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8742A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8742A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30660A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22629A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.906A>G
  hgvsp: ENST00000380572.3:c.906A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22629A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8742A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30660A>G
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 2.5e0
  variant carriers: 390
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 153
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.75e1
  variant carriers: 198
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 2.25e1
  variant carriers: 212
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.25e1
  variant carriers: 262
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 647
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 216
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 6.25e1
  variant carriers: 496
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.75e1
  variant carriers: 377
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 159
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 245
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.25e1
  variant carriers: 556
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 369
genotype quality: GenotypeQuality
hgvs: p.Glu302Glu
num of homozygotes: 1979
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

8-26636927-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636927
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636927
    reference: chr 8
allele count: 1
allele frequency: 7.390983000739098e-5
allele num: 13530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8744G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8744G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22631G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8744G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.904G>A
  hgvsp: ENSP00000369946.3:p.Glu302Lys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8744G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8744G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30662G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30662G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8744G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8744G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22631G>A
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu302Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

8-26636945-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636945
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636945
    reference: chr 8
allele count: 1
allele frequency: 7.67341927562922e-5
allele num: 13032
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8762G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8762G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8762G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30680G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.886G>A
  hgvsp: ENSP00000369946.3:p.Glu296Lys
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8762G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8762G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30680G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8762G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22649G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8762G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22649G>A
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu296Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/8-26636970-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636970
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636970
    reference: chr 8
allele count: 37
allele frequency: 3.045768850839644e-3
allele num: 12148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8787G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30705G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.884-23G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8787G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8787G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30705G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8787G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22674G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22674G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8787G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8787G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8787G>T
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 1.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

8-26636981-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636981
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636981
    reference: chr 8
allele count: 3368
allele frequency: 2.853270077939681e-1
allele num: 11804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22685C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8798C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30716C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8798C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22685C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8798C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.884-34C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8798C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30716C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8798C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8798C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8798C>T
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 2.25e1
  variant carriers: 754
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 2.5e0
  variant carriers: 159
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 7.5e0
  variant carriers: 285
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 2.75e1
  variant carriers: 463
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 1.75e1
  variant carriers: 766
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 1.25e1
  variant carriers: 468
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 3.75e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.25e1
  variant carriers: 197
genotype quality: GenotypeQuality
num of homozygotes: 492
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

8-26636985-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26636985
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26636985
    reference: chr 8
allele count: 1
allele frequency: 8.950948800572861e-5
allele num: 11172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*83-22689G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.884-22689G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.884-8802G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl transcript: ENST00000518621
  gene symbol: ADRA1A
  hgvsc: ENST00000518621.1:n.97-8802G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.884-38G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.884-8802G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.884-8802G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.884-8802G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.884-8802G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.884-30720G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.884-8802G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*83-30720G>A
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

8-26716582-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716582
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716582
    reference: chr 8
allele count: 8
allele frequency: 5.815644082582146e-4
allele num: 13756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+5022C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+5022C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+5022C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+5022C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+5022C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+5022C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*49C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+5022C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*49C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+5022C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+5022C>T
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-26716597-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716597
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716597
    reference: chr 8
allele count: 14
allele frequency: 1.005458201666188e-3
allele num: 13924
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*34T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+5007T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+5007T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+5007T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*34T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+5007T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+5007T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+5007T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+5007T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+5007T>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+5007T>A
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

8-26716611-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716611
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716611
    reference: chr 8
allele count: 43
allele frequency: 3.041878890775325e-3
allele num: 14136
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4993G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4993G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*20G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*20G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4993G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4993G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4993G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4993G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4993G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4993G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4993G>A
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

8-26716613-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716613
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716613
    reference: chr 8
allele count: 1
allele frequency: 7.036307345904869e-5
allele num: 14212
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4991G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4991G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*18G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4991G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4991G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*18G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4991G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4991G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4991G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4991G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4991G>A
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum

8-26716619-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716619
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716619
    reference: chr 8
allele count: 2
allele frequency: 1.392757660167131e-4
allele num: 14360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4985G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4985G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4985G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4985G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*12G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*12G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4985G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4985G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4985G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4985G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4985G>A
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

8-26716622-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716622
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716622
    reference: chr 8
allele count: 1649
allele frequency: 1.13146699602031e-1
allele num: 14574
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4982C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*9C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4982C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4982C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4982C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4982C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*9C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4982C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4982C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4982C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4982C>T
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 2.5e0
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 3.75e1
  variant carriers: 223
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.5e0
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 3.25e1
  variant carriers: 259
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 2.25e1
  variant carriers: 156
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.25e1
  variant carriers: 162
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 2.75e1
  variant carriers: 223
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 2
num of homozygotes: 107
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-26716628-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716628
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716628
    reference: chr 8
allele count: 1
allele frequency: 6.815703380588877e-5
allele num: 14672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4976C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.*3C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.*3C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4976C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4976C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4976C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4976C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4976C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4976C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4976C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4976C>T
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP

8-26716633-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716633
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716633
    reference: chr 8
allele count: 100
allele frequency: 6.775067750677507e-3
allele num: 14760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4971T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4971T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4971T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.973T>C
  hgvsp: ENSP00000431073.1:p.Ter325ArgextTer12
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.973T>C
  hgvsp: ENSP00000430414.1:p.Ter325ArgextTer12
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4971T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4971T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4971T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4971T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000351725
  ensembl transcript: ENST00000358857
  gene symbol: ADRA1A
  hgvsc: ENST00000358857.5:c.973T>C
  hgvsp: ENSP00000351725.5:p.Ter325ArgextTer?
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4971T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4971T>C
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter325ArgextTer?
num of homozygotes: 2
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

8-26716642-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716642
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716642
    reference: chr 8
allele count: 654
allele frequency: 4.388672661387733e-2
allele num: 14902
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.964A>G
  hgvsp: ENSP00000431073.1:p.Ile322Val
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4962A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4962A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4962A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4962A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.964A>G
  hgvsp: ENSP00000430414.1:p.Ile322Val
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4962A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000351725
  ensembl transcript: ENST00000358857
  gene symbol: ADRA1A
  hgvsc: ENST00000358857.5:c.964A>G
  hgvsp: ENSP00000351725.5:p.Ile322Val
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4962A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4962A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4962A>G
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4962A>G
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.5e0
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 2.5e0
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 3.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 2.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
hgvs: p.Ile322Val
num of homozygotes: 15
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

8-26716655-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716655
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716655
    reference: chr 8
allele count: 18
allele frequency: 1.201441730076091e-3
allele num: 14982
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4949G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.951G>A
  hgvsp: ENST00000519096.1:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000351725
  ensembl transcript: ENST00000358857
  gene symbol: ADRA1A
  hgvsc: ENST00000358857.5:c.951G>A
  hgvsp: ENST00000358857.5:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.951G>A
  hgvsp: ENST00000521711.1:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4949G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4949G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4949G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4949G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4949G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4949G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4949G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4949G>A
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg317Arg
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

8-26716657-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716657
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716657
    reference: chr 8
allele count: 1
allele frequency: 6.673785371062466e-5
allele num: 14984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4947C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.949C>A
  hgvsp: ENST00000519096.1:c.949C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4947C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4947C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.949C>A
  hgvsp: ENST00000521711.1:c.949C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4947C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4947C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4947C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000351725
  ensembl transcript: ENST00000358857
  gene symbol: ADRA1A
  hgvsc: ENST00000358857.5:c.949C>A
  hgvsp: ENST00000358857.5:c.949C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4947C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4947C>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4947C>A
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg317Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

8-26716661-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716661
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716661
    reference: chr 8
allele count: 1
allele frequency: 6.657789613848202e-5
allele num: 15020
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4943G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4943G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4943G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4943G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000351725
  ensembl transcript: ENST00000358857
  gene symbol: ADRA1A
  hgvsc: ENST00000358857.5:c.945G>A
  hgvsp: ENST00000358857.5:c.945G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4943G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.945G>A
  hgvsp: ENST00000519096.1:c.945G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4943G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4943G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.945G>A
  hgvsp: ENST00000521711.1:c.945G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4943G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4943G>A
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg315Arg
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

8-26716673-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716673
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716673
    reference: chr 8
allele count: 1
allele frequency: 6.652474720596061e-5
allele num: 15032
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4931G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4931G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4931G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000351725
  ensembl transcript: ENST00000358857
  gene symbol: ADRA1A
  hgvsc: ENST00000358857.5:c.933G>A
  hgvsp: ENST00000358857.5:c.933G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4931G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.933G>A
  hgvsp: ENST00000521711.1:c.933G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4931G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4931G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4931G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4931G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.933G>A
  hgvsp: ENST00000519096.1:c.933G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4931G>A
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser311Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

8-26716680-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716680
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716680
    reference: chr 8
allele count: 1
allele frequency: 6.648936170212766e-5
allele num: 15040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.926G>A
  hgvsp: ENSP00000431073.1:p.Gly309Glu
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4924G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4924G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4924G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4924G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000351725
  ensembl transcript: ENST00000358857
  gene symbol: ADRA1A
  hgvsc: ENST00000358857.5:c.926G>A
  hgvsp: ENSP00000351725.5:p.Gly309Glu
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4924G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.926G>A
  hgvsp: ENSP00000430414.1:p.Gly309Glu
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4924G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4924G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4924G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4924G>A
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly309Glu
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

8-26716699-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716699
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716699
    reference: chr 8
allele count: 20
allele frequency: 1.334578940344321e-3
allele num: 14986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.907G>A
  hgvsp: ENSP00000431073.1:p.Val303Met
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4905G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4905G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.907G>A
  hgvsp: ENSP00000430414.1:p.Val303Met
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4905G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4905G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4905G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000351725
  ensembl transcript: ENST00000358857
  gene symbol: ADRA1A
  hgvsc: ENST00000358857.5:c.907G>A
  hgvsp: ENSP00000351725.5:p.Val303Met
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4905G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4905G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4905G>A
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4905G>A
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val303Met
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

8-26716703-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716703
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716703
    reference: chr 8
allele count: 11
allele frequency: 7.354907729339395e-4
allele num: 14956
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4901T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4901T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4901T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000351725
  ensembl transcript: ENST00000358857
  gene symbol: ADRA1A
  hgvsc: ENST00000358857.5:c.903T>C
  hgvsp: ENST00000358857.5:c.903T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.903T>C
  hgvsp: ENST00000521711.1:c.903T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4901T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4901T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4901T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4901T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.903T>C
  hgvsp: ENST00000519096.1:c.903T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4901T>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4901T>C
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr301Tyr
num of homozygotes: 1
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

8-26716715-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716715
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716715
    reference: chr 8
allele count: 1674
allele frequency: 1.126665769282541e-1
allele num: 14858
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.891C>T
  hgvsp: ENST00000519096.1:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4889C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000351725
  ensembl transcript: ENST00000358857
  gene symbol: ADRA1A
  hgvsc: ENST00000358857.5:c.891C>T
  hgvsp: ENST00000358857.5:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.891C>T
  hgvsp: ENST00000521711.1:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4889C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4889C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4889C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4889C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4889C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4889C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4889C>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4889C>T
  variant of: http://identifiers.org/hgnc/277
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.75e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.5e0
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 2.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 3.25e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.75e1
  variant carriers: 183
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.75e1
  variant carriers: 159
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 2.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 2.5e0
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.25e1
  variant carriers: 231
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 184
genotype quality: GenotypeQuality
hgvs: p.Tyr297Tyr
num of homozygotes: 110
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

8-26716750-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26716750
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26716750
    reference: chr 8
allele count: 26
allele frequency: 1.849743881616391e-3
allele num: 14056
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+4854A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.884-28A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000346557
  ensembl transcript: ENST00000354550
  gene symbol: ADRA1A
  hgvsc: ENST00000354550.4:c.883+4854A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369961
  ensembl transcript: ENST00000380587
  gene symbol: ADRA1A
  hgvsc: ENST00000380587.1:c.883+4854A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.884-28A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+4854A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000351725
  ensembl transcript: ENST00000358857
  gene symbol: ADRA1A
  hgvsc: ENST00000358857.5:c.884-28A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+4854A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369960
  ensembl transcript: ENST00000380586
  gene symbol: ADRA1A
  hgvsc: ENST00000380586.1:c.883+4854A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000276393
  ensembl transcript: ENST00000276393
  gene symbol: ADRA1A
  hgvsc: ENST00000276393.4:c.883+4854A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+4854A>C
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+4854A>C
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/8-26721551-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26721551
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 26721551
    reference: chr 8
allele count: 5445
allele frequency: 5.181864900359733e-2
allele num: 105078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369946
  ensembl transcript: ENST00000380572
  gene symbol: ADRA1A
  hgvsc: ENST00000380572.3:c.883+53G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369955
  ensembl transcript: ENST00000380581
  gene symbol: ADRA1A
  hgvsc: ENST00000380581.2:c.883+53G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000431073
  ensembl transcript: ENST00000519096
  gene symbol: ADRA1A
  hgvsc: ENST00000519096.1:c.883+53G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430414
  ensembl transcript: ENST00000521711
  gene symbol: ADRA1A
  hgvsc: ENST00000521711.1:c.883+53G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369956
  ensembl transcript: ENST00000380582
  gene symbol: ADRA1A
  hgvsc: ENST00000380582.3:c.883+53G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000369947
  ensembl transcript: ENST00000380573
  gene symbol: ADRA1A
  hgvsc: ENST00000380573.3:c.883+53G>T
  variant of: http://identifiers.org/hgnc/277
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120907
  ensembl protein: ENSP00000430793
  ensembl transcript: ENST00000519229
  gene symbol: ADRA1A
  hgvsc: ENST00000519229.1:c.883+53G>T
  variant of: http://identifiers.org/hgnc/277
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 330
reference allele: C

GenotypeDepth
all individuals: 57
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40528
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2638
bin: 9.75e1
variant carriers: 19

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

GenotypeQuality
all individuals: 556
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2426
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 68
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2622
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9725
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1407
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 9.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 19
allele frequency: 1.835748792270531e-3
allele num: 10350
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.839242e6

VQSLOD
type: SiteQuality
SIO_000300: 5.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.47e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.253e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.249e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.66e-1

GenotypeDepth
all individuals: 57
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 556
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 75
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9725
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40536
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2623
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2620
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2422
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 8.25e1
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: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
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: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.83626e6

MQ
type: SiteQuality
SIO_000300: 5.949e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.906e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

MQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

QD
type: SiteQuality
SIO_000300: 1.344e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

GenotypeDepth
all individuals: 3356
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 79
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9726
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1408
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2422
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2619
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40535
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2622
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.836017e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.283e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

FS
type: SiteQuality
SIO_000300: 1.142e0

MQRankSum
type: SiteQuality
SIO_000300: -1.089e0

VQSLOD
type: SiteQuality
SIO_000300: 1.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

GenotypeDepth
all individuals: 461
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9715
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40502
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2620
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2416
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1403
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 121
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2618
bin: 9.75e1
variant carriers: 1

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
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: 16512
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.479e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.108e0

QD
type: SiteQuality
SIO_000300: 1.115e1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.961e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

DP
type: SiteQuality
SIO_000300: 1.834984e6

GenotypeDepth
all individuals: 669
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 177
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2610
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1394
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40449
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2615
bin: 9.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 555
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9708
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.341e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
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SIO_000300: 6.5e-1

ReadPosRankSum
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SIO_000300: 1.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

DP
type: SiteQuality
SIO_000300: 1.833621e6

FS
type: SiteQuality
SIO_000300: 1.288e0

BaseQRankSum
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SIO_000300: -3.025e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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

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

Other
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.49829064955317e-5
allele num: 66692
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

ReadPosRankSum
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MQ
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SIO_000300: 5.955e1

DP
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FS
type: SiteQuality
SIO_000300: 6.27e-1

QD
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VQSLOD
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BaseQRankSum
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SIO_000300: -6.346e0

InbreedingCoeff
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SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.34e-1

GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele 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

DP
type: SiteQuality
SIO_000300: 1.830141e6

QD
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BaseQRankSum
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SIO_000300: 4.82e0

MQRankSum
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SIO_000300: -3.6e-2

ClippingRankSum
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SIO_000300: -1.83e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.948e1

FS
type: SiteQuality
SIO_000300: 1.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.23e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

Other
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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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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European (Non-Finnish)
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allele count: 1
allele frequency: 1.503036132988637e-5
allele num: 66532
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.334000000000001e-1

QD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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SIO_000300: 6.01e-1

ClippingRankSum
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SIO_000300: -5.34e-1

DP
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SIO_000300: 1.824914e6

MQRankSum
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SIO_000300: 8.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -4.01e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9986
num of homozygotes: 0

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

South Asian
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allele num: 16496
num of homozygotes: 0

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

InbreedingCoeff
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VQSLOD
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ClippingRankSum
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FS
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ReadPosRankSum
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QD
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DP
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MQRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

African
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allele count: 2
allele frequency: 2.014098690835851e-4
allele num: 9930
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 6
allele frequency: 9.029617144233085e-5
allele num: 66448
num of homozygotes: 0

Other
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FS
type: SiteQuality
SIO_000300: 7.41e-1

ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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MQ
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ClippingRankSum
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QD
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GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505706628120577e-5
allele num: 66414
num of homozygotes: 0

Latino
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South Asian
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Other
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European (Finnish)
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African
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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DP
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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FS
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 551
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

Other
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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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allele num: 66366
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East Asian
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FS
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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ClippingRankSum
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MQ
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QD
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MQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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South Asian
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Latino
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Other
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European (Finnish)
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MQ
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DP
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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FS
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66192
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European (Finnish)
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Latino
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South Asian
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African
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East Asian
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Other
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VQSLOD
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MQ
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FS
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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ClippingRankSum
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QD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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East Asian
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Other
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South Asian
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MQ
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ClippingRankSum
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MQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

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

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

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531956614988664e-5
allele num: 65276
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15314
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8412
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.726e0

VQSLOD
type: SiteQuality
SIO_000300: 4.86e-1

FS
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SIO_000300: 0.0e0

DP
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SIO_000300: 1.760134e6

QD
type: SiteQuality
SIO_000300: 1.468e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

GenotypeDepth
all individuals: 633
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2857
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 672
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.052188552188552e-4
allele num: 9504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15152
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65132
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.349e1

MQRankSum
type: SiteQuality
SIO_000300: -4.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.38e-1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 1.826e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.208e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.385e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 2307
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14284
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555451858764971e-5
allele num: 64290
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.708244e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.733e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.73e0

FS
type: SiteQuality
SIO_000300: 5.027e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.66e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.589e0

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

QD
type: SiteQuality
SIO_000300: 1.205e1

MQ
type: SiteQuality
SIO_000300: 5.347e1

GenotypeDepth
all individuals: 443
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2519
bin: 9.75e1
variant carriers: 12

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 646
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variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 1.284521515735388e-3
allele num: 9342
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63936
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14000
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.447e1

VQSLOD
type: SiteQuality
SIO_000300: 3.49e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.1e-1

FS
type: SiteQuality
SIO_000300: 1.941e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

DP
type: SiteQuality
SIO_000300: 1.68857e6

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1670
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8671
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6140
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7978
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11184
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61812
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.233139794551139e-4
allele num: 8956
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.492e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

BaseQRankSum
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SIO_000300: 3.37e0

MQ
type: SiteQuality
SIO_000300: 5.728e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.514053e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

QD
type: SiteQuality
SIO_000300: 1.508e1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7978
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11198
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.117068811438785e-4
allele num: 8952
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12430
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.99e-1

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

DP
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VQSLOD
type: SiteQuality
SIO_000300: -5.147e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.36e-1

FS
type: SiteQuality
SIO_000300: 2.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

QD
type: SiteQuality
SIO_000300: 1.862e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.622586402725945e-5
allele num: 61630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8932
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

MQ
type: SiteQuality
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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MQRankSum
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BaseQRankSum
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FS
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QD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3386
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variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.792114695340502e-4
allele num: 11160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61594
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7958
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8918
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -9.163e-1

DP
type: SiteQuality
SIO_000300: 1.475997e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

FS
type: SiteQuality
SIO_000300: 5.456e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

ClippingRankSum
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SIO_000300: -8.120000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.873e1

QD
type: SiteQuality
SIO_000300: 1.357e1

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11150
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8890
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.628558400104228e-5
allele num: 61404
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11994
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7938
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ReadPosRankSum
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SIO_000300: -3.97e-1

BaseQRankSum
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SIO_000300: 1.05e0

FS
type: SiteQuality
SIO_000300: 2.285e0

VQSLOD
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SIO_000300: 2.37e-1

MQ
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SIO_000300: 5.932e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.62e-1

DP
type: SiteQuality
SIO_000300: 1.451264e6

MQRankSum
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QD
type: SiteQuality
SIO_000300: 1.119e1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10980
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7726
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10800
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.672073036150219e-5
allele num: 59806
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8666
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.617e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.34e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.853e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.028e0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.664e0

DP
type: SiteQuality
SIO_000300: 1.304138e6

QD
type: SiteQuality
SIO_000300: 1.999e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10580
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.196247930844215e-5
allele num: 10874
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7626
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.278896e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

QD
type: SiteQuality
SIO_000300: 5.51e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10700
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.29e-1

BaseQRankSum
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SIO_000300: 3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.62e-1

DP
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SIO_000300: 1.270952e6

MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: -1.159e0

QD
type: SiteQuality
SIO_000300: 1.107e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.561524047470331e-4
allele num: 6404
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

DP
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SIO_000300: 1.78028e5

QD
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VQSLOD
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SIO_000300: -7.877e-1

InbreedingCoeff
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SIO_000300: -2.53e-2

ClippingRankSum
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SIO_000300: -1.758e0

BaseQRankSum
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SIO_000300: -1.516e0

FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 104

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

South Asian
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allele count: 65
allele frequency: 1.155761024182077e-2
allele num: 5624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 38
allele frequency: 1.20942075111394e-2
allele num: 3142
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 6.172839506172839e-3
allele num: 162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 2.512562814070352e-3
allele num: 1592
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 5.703422053231939e-3
allele num: 526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

ReadPosRankSum
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FS
type: SiteQuality
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MQRankSum
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QD
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 6.035e1

InbreedingCoeff
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SIO_000300: 4.33e-2

DP
type: SiteQuality
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BaseQRankSum
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SIO_000300: 6.900000000000001e-2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.273074474856779e-3
allele num: 3142
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

South Asian
type: Population
allele count: 17
allele frequency: 3.02275960170697e-3
allele num: 5624
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.33e-2

DP
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SIO_000300: 1.92902e5

GenotypeDepth
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variant carriers: 0

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

South Asian
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East Asian
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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 (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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FS
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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MQ
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -2.87e-2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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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 frequency: 0.0e0
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MQ
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SIO_000300: 6.0e1

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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ClippingRankSum
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FS
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

East Asian
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Other
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num of homozygotes: 0

African
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num of homozygotes: 0

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

QD
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQ
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DP
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FS
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ClippingRankSum
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MQRankSum
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GenotypeDepth
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variant carriers: 5

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 15

European (Non-Finnish)
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allele count: 3
allele frequency: 7.739938080495357e-4
allele num: 3876
num of homozygotes: 0

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

South Asian
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allele frequency: 1.443948542924652e-3
allele num: 7618
num of homozygotes: 0

Latino
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East Asian
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Other
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num of homozygotes: 0

ReadPosRankSum
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FS
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BaseQRankSum
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QD
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MQ
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DP
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.586652871184687e-4
allele num: 3866
num of homozygotes: 0

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

Latino
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European (Non-Finnish)
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African
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East Asian
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Other
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South Asian
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MQ
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MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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FS
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InbreedingCoeff
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BaseQRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 67

GenotypeQuality
all individuals: 41
bin: 3.25e1
variant carriers: 10

GenotypeQuality
all individuals: 165
bin: 2.25e1
variant carriers: 11

GenotypeQuality
all individuals: 93
bin: 9.25e1
variant carriers: 10

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 20

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 24

GenotypeQuality
all individuals: 217
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2702
bin: 6.25e1
variant carriers: 11

GenotypeQuality
all individuals: 569
bin: 6.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2719
bin: 9.75e1
variant carriers: 2225

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 6

Latino
type: Population
allele count: 27
allele frequency: 1.436170212765958e-1
allele num: 188
num of homozygotes: 1

African
type: Population
allele count: 103
allele frequency: 1.832740213523132e-1
allele num: 562
num of homozygotes: 10

European (Non-Finnish)
type: Population
allele count: 449
allele frequency: 1.160806618407446e-1
allele num: 3868
num of homozygotes: 22

East Asian
type: Population
allele count: 91
allele frequency: 4.55e-1
allele num: 200
num of homozygotes: 20

Other
type: Population
allele count: 28
allele frequency: 1.521739130434783e-1
allele num: 184
num of homozygotes: 3

South Asian
type: Population
allele count: 1590
allele frequency: 2.087161984772906e-1
allele num: 7618
num of homozygotes: 184

European (Finnish)
type: Population
allele count: 199
allele frequency: 1.310935441370224e-1
allele num: 1518
num of homozygotes: 11

FS
type: SiteQuality
SIO_000300: 1.269e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

QD
type: SiteQuality
SIO_000300: 1.557e1

VQSLOD
type: SiteQuality
SIO_000300: 4.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.07e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

DP
type: SiteQuality
SIO_000300: 2.97439e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.27e-1

GenotypeDepth
all individuals: 334
bin: 4.75e1
variant carriers: 4

GenotypeDepth
all individuals: 337
bin: 4.25e1
variant carriers: 8

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

GenotypeQuality
all individuals: 84
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1913
bin: 9.75e1
variant carriers: 110

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1964
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 73
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 201
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 383
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2573
bin: 6.25e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 57
allele frequency: 1.482059282371295e-2
allele num: 3846
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 33
allele frequency: 2.301255230125523e-2
allele num: 1434
num of homozygotes: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.571428571428571e-3
allele num: 560
num of homozygotes: 0

South Asian
type: Population
allele count: 17
allele frequency: 2.232142857142857e-3
allele num: 7616
num of homozygotes: 1

Other
type: Population
allele count: 4
allele frequency: 2.197802197802198e-2
allele num: 182
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.729e1

MQRankSum
type: SiteQuality
SIO_000300: -1.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.5e-2

DP
type: SiteQuality
SIO_000300: 2.60122e5

MQ
type: SiteQuality
SIO_000300: 5.811e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

FS
type: SiteQuality
SIO_000300: 1.468e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.12e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.69e-1

GenotypeDepth
all individuals: 688
bin: 5.25e1
variant carriers: 683

GenotypeDepth
all individuals: 593
bin: 5.75e1
variant carriers: 588

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 29

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 19

GenotypeQuality
all individuals: 272
bin: 2.25e1
variant carriers: 47

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 18

GenotypeQuality
all individuals: 5167
bin: 9.75e1
variant carriers: 5119

GenotypeQuality
all individuals: 970
bin: 7.5e0
variant carriers: 222

GenotypeQuality
all individuals: 116
bin: 1.75e1
variant carriers: 106

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 19

GenotypeQuality
all individuals: 1220
bin: 6.25e1
variant carriers: 35

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 21

GenotypeQuality
all individuals: 410
bin: 2.5e0
variant carriers: 17

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 23

GenotypeQuality
all individuals: 191
bin: 6.75e1
variant carriers: 33

GenotypeQuality
all individuals: 51
bin: 8.25e1
variant carriers: 30

GenotypeQuality
all individuals: 46
bin: 9.25e1
variant carriers: 35

GenotypeQuality
all individuals: 118
bin: 1.25e1
variant carriers: 104

GenotypeQuality
all individuals: 57
bin: 7.75e1
variant carriers: 20

GenotypeQuality
all individuals: 45
bin: 7.25e1
variant carriers: 16

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 12

European (Finnish)
type: Population
allele count: 550
allele frequency: 4.092261904761905e-1
allele num: 1344
num of homozygotes: 91

European (Non-Finnish)
type: Population
allele count: 1866
allele frequency: 4.859375e-1
allele num: 3840
num of homozygotes: 453

Latino
type: Population
allele count: 101
allele frequency: 5.372340425531915e-1
allele num: 188
num of homozygotes: 25

African
type: Population
allele count: 411
allele frequency: 7.313167259786477e-1
allele num: 562
num of homozygotes: 153

East Asian
type: Population
allele count: 185
allele frequency: 9.343434343434344e-1
allele num: 198
num of homozygotes: 86

Other
type: Population
allele count: 96
allele frequency: 5.393258426966292e-1
allele num: 178
num of homozygotes: 28

South Asian
type: Population
allele count: 4089
allele frequency: 5.370370370370371e-1
allele num: 7614
num of homozygotes: 1143

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

DP
type: SiteQuality
SIO_000300: 3.22127e5

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e0

VQSLOD
type: SiteQuality
SIO_000300: 6.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

QD
type: SiteQuality
SIO_000300: 2.294e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.401e-1

FS
type: SiteQuality
SIO_000300: 7.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

GenotypeDepth
all individuals: 246
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 681
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2039
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4521
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 60
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 82
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.31891321551042e-4
allele num: 7582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1076
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.91187e5

MQRankSum
type: SiteQuality
SIO_000300: 7.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.95e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.671e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

QD
type: SiteQuality
SIO_000300: 1.47e1

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1028
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2112
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3961
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.343724805159903e-4
allele num: 7442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3666
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.78521e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.06e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.55e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.501e0

VQSLOD
type: SiteQuality
SIO_000300: -5.825e-1

QD
type: SiteQuality
SIO_000300: 1.09e1

GenotypeDepth
all individuals: 23
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 158
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2527
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1863
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 46
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1308
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 106
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 64
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 96
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 367
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 268
bin: 9.75e1
variant carriers: 38

GenotypeQuality
all individuals: 223
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 395
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 145
bin: 7.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 21
allele frequency: 4.929577464788732e-2
allele num: 426
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.399384270920795e-4
allele num: 7146
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 4.280821917808219e-3
allele num: 3504
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 1.387e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.902e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.65e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.46626e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 60
bin: 8.75e1
variant carriers: 45

GenotypeQuality
all individuals: 111
bin: 7.75e1
variant carriers: 70

GenotypeQuality
all individuals: 205
bin: 6.75e1
variant carriers: 85

GenotypeQuality
all individuals: 847
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 3.75e1
variant carriers: 40

GenotypeQuality
all individuals: 79
bin: 7.25e1
variant carriers: 39

GenotypeQuality
all individuals: 2481
bin: 9.75e1
variant carriers: 2385

GenotypeQuality
all individuals: 67
bin: 9.25e1
variant carriers: 47

GenotypeQuality
all individuals: 169
bin: 4.25e1
variant carriers: 27

GenotypeQuality
all individuals: 355
bin: 2.75e1
variant carriers: 43

GenotypeQuality
all individuals: 719
bin: 6.25e1
variant carriers: 78

GenotypeQuality
all individuals: 149
bin: 1.75e1
variant carriers: 47

GenotypeQuality
all individuals: 958
bin: 2.25e1
variant carriers: 47

GenotypeQuality
all individuals: 1831
bin: 7.5e0
variant carriers: 84

GenotypeQuality
all individuals: 76
bin: 8.25e1
variant carriers: 46

GenotypeQuality
all individuals: 173
bin: 1.25e1
variant carriers: 38

GenotypeQuality
all individuals: 150
bin: 4.75e1
variant carriers: 51

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 40

GenotypeQuality
all individuals: 550
bin: 3.25e1
variant carriers: 55

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 58

European (Finnish)
type: Population
allele count: 58
allele frequency: 2.357723577235772e-1
allele num: 246
num of homozygotes: 7

Other
type: Population
allele count: 45
allele frequency: 3.358208955223881e-1
allele num: 134
num of homozygotes: 9

African
type: Population
allele count: 177
allele frequency: 3.241758241758242e-1
allele num: 546
num of homozygotes: 25

East Asian
type: Population
allele count: 20
allele frequency: 1.041666666666667e-1
allele num: 192
num of homozygotes: 0

Latino
type: Population
allele count: 59
allele frequency: 3.138297872340425e-1
allele num: 188
num of homozygotes: 7

European (Non-Finnish)
type: Population
allele count: 1143
allele frequency: 3.318815331010453e-1
allele num: 3444
num of homozygotes: 179

South Asian
type: Population
allele count: 1866
allele frequency: 2.645307626878367e-1
allele num: 7054
num of homozygotes: 265

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.52e0

DP
type: SiteQuality
SIO_000300: 1.37427e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.608e0

QD
type: SiteQuality
SIO_000300: 1.683e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

African
type: Population
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allele frequency: 1.824817518248175e-3
allele num: 548
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3292
num of homozygotes: 0

East Asian
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South Asian
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VQSLOD
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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SIO_000300: -1.803e0

QD
type: SiteQuality
SIO_000300: 8.529999999999999e0

DP
type: SiteQuality
SIO_000300: 1.22842e5

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1602
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3878
num of homozygotes: 0

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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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 1.127078050154973e-3
allele num: 7098
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Other
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allele frequency: 0.0e0
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QD
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SIO_000300: 1.342e1

MQ
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FS
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MQRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -4.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.22e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 1.870324189526184e-3
allele num: 1604
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.623376623376623e-3
allele num: 616
num of homozygotes: 0

South Asian
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allele count: 4
allele frequency: 5.532503457814661e-4
allele num: 7230
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 1.53217568947906e-3
allele num: 3916
num of homozygotes: 0

FS
type: SiteQuality
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DP
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MQ
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.36e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 42

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4012
num of homozygotes: 0

South Asian
type: Population
allele count: 43
allele frequency: 5.864702673213312e-3
allele num: 7332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 622
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1606
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-1

BaseQRankSum
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SIO_000300: -2.822e0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

FS
type: SiteQuality
SIO_000300: 9.05e-1

QD
type: SiteQuality
SIO_000300: 1.346e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.79e-1

DP
type: SiteQuality
SIO_000300: 1.97122e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.22e-2

GenotypeQuality
all individuals: 110
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 6.226650062266501e-4
allele num: 1606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 196
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7388
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4024
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.36e-1

FS
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SIO_000300: 6.335e0

BaseQRankSum
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SIO_000300: -3.11e0

ReadPosRankSum
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SIO_000300: 1.76e-1

ClippingRankSum
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SIO_000300: -5.05e-1

DP
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SIO_000300: 1.98497e5

InbreedingCoeff
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SIO_000300: -2.02e-2

MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
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MQRankSum
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SIO_000300: -1.537e0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1608
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 2.683123155352831e-4
allele num: 7454
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 640
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4092
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.05e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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ClippingRankSum
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MQRankSum
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QD
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DP
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BaseQRankSum
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SIO_000300: 1.36e0

GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 14

Latino
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allele count: 33
allele frequency: 1.793478260869565e-1
allele num: 184
num of homozygotes: 3

African
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allele count: 103
allele frequency: 1.555891238670695e-1
allele num: 662
num of homozygotes: 6

East Asian
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allele count: 31
allele frequency: 1.565656565656566e-1
allele num: 198
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European (Non-Finnish)
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allele count: 607
allele frequency: 1.441120607787275e-1
allele num: 4212
num of homozygotes: 45

European (Finnish)
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allele count: 113
allele frequency: 7.027363184079602e-2
allele num: 1608
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South Asian
type: Population
allele count: 742
allele frequency: 9.85653560042508e-2
allele num: 7528
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Other
type: Population
allele count: 20
allele frequency: 1.098901098901099e-1
allele num: 182
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DP
type: SiteQuality
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QD
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VQSLOD
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FS
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MQRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.29e-2

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4258
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
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South Asian
type: Population
allele count: 1
allele frequency: 1.322751322751323e-4
allele num: 7560
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.585000000000001e0

InbreedingCoeff
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.289e0

VQSLOD
type: SiteQuality
SIO_000300: -3.428e-1

QD
type: SiteQuality
SIO_000300: 1.219e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

DP
type: SiteQuality
SIO_000300: 2.24827e5

GenotypeDepth
all individuals: 17
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 504
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variant carriers: 15

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 297
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1276
bin: 9.75e1
variant carriers: 96

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 222
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GenotypeQuality
all individuals: 319
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.052631578947368e-2
allele num: 190
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

South Asian
type: Population
allele count: 98
allele frequency: 1.291512915129151e-2
allele num: 7588
num of homozygotes: 1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

DP
type: SiteQuality
SIO_000300: 2.2795e5

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.64e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.261e1

VQSLOD
type: SiteQuality
SIO_000300: 4.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.425e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 82
bin: 6.75e1
variant carriers: 47

GenotypeDepth
all individuals: 43
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variant carriers: 16

GenotypeQuality
all individuals: 1380
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GenotypeQuality
all individuals: 61
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variant carriers: 4

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 4

GenotypeQuality
all individuals: 278
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GenotypeQuality
all individuals: 503
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GenotypeQuality
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GenotypeQuality
all individuals: 1684
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variant carriers: 633

GenotypeQuality
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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

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 640
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GenotypeQuality
all individuals: 142
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variant carriers: 4

GenotypeQuality
all individuals: 3852
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variant carriers: 2

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 203
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 218
allele frequency: 4.952294411631077e-2
allele num: 4402
num of homozygotes: 3

European (Finnish)
type: Population
allele count: 105
allele frequency: 6.473489519112208e-2
allele num: 1622
num of homozygotes: 4

Latino
type: Population
allele count: 3
allele frequency: 1.578947368421053e-2
allele num: 190
num of homozygotes: 0

South Asian
type: Population
allele count: 310
allele frequency: 4.07465825446898e-2
allele num: 7608
num of homozygotes: 8

African
type: Population
allele count: 12
allele frequency: 1.724137931034483e-2
allele num: 696
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 3.225806451612903e-2
allele num: 186
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

QD
type: SiteQuality
SIO_000300: 1.475e1

DP
type: SiteQuality
SIO_000300: 2.4342e5

VQSLOD
type: SiteQuality
SIO_000300: 6.42e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeDepth
all individuals: 2838
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variant carriers: 0

GenotypeDepth
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 152
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 735
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GenotypeQuality
all individuals: 27
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1534
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GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 224
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 311
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.434782608695652e-3
allele num: 184
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 2.017032720753026e-3
allele num: 4462
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 1.050420168067227e-3
allele num: 7616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1624
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.82e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.30887e5

MQRankSum
type: SiteQuality
SIO_000300: -1.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.05e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

QD
type: SiteQuality
SIO_000300: 1.231e1

VQSLOD
type: SiteQuality
SIO_000300: 4.02e0

GenotypeDepth
all individuals: 11
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 631
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 147
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GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 1442
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GenotypeQuality
all individuals: 741
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 1141
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GenotypeQuality
all individuals: 4247
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 283
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GenotypeQuality
all individuals: 307
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GenotypeQuality
all individuals: 240
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GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
all individuals: 224
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GenotypeQuality
all individuals: 152
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.313025210084034e-4
allele num: 7616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.596000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

MQ
type: SiteQuality
SIO_000300: 5.891e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.18e-1

QD
type: SiteQuality
SIO_000300: 9.49e0

FS
type: SiteQuality
SIO_000300: 4.342e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.66e-1

DP
type: SiteQuality
SIO_000300: 2.30401e5

GenotypeDepth
all individuals: 19
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variant carriers: 0

GenotypeDepth
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 1531
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 283
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GenotypeQuality
all individuals: 116
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GenotypeQuality
all individuals: 6
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 1141
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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: 5
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GenotypeQuality
all individuals: 152
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GenotypeQuality
all individuals: 310
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GenotypeQuality
all individuals: 741
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GenotypeQuality
all individuals: 224
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.281e0

MQRankSum
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SIO_000300: 1.74e0

ReadPosRankSum
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SIO_000300: -1.018e0

VQSLOD
type: SiteQuality
SIO_000300: -9.932e-1

DP
type: SiteQuality
SIO_000300: 2.30716e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.75e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.743e0

QD
type: SiteQuality
SIO_000300: 1.008e1

MQ
type: SiteQuality
SIO_000300: 5.947e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

GenotypeDepth
all individuals: 32
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 19
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GenotypeQuality
all individuals: 25
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GenotypeQuality
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GenotypeQuality
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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: 691
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GenotypeQuality
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 308
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 224
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GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4279
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.388e0

MQRankSum
type: SiteQuality
SIO_000300: 5.49e-1

FS
type: SiteQuality
SIO_000300: 8.619999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 5.726e1

DP
type: SiteQuality
SIO_000300: 2.30843e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.64e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.294e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.360000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.242e1

GenotypeDepth
all individuals: 10
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variant carriers: 0

GenotypeDepth
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 121
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GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 1430
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 241
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 1141
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 3.75e1
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GenotypeQuality
all individuals: 151
bin: 8.75e1
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GenotypeQuality
all individuals: 283
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4275
bin: 6.25e1
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GenotypeQuality
all individuals: 746
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
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variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
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variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.67e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 5.796e1

DP
type: SiteQuality
SIO_000300: 2.30652e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.251e0

FS
type: SiteQuality
SIO_000300: 5.649e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

VQSLOD
type: SiteQuality
SIO_000300: -3.811e0

QD
type: SiteQuality
SIO_000300: 6.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.942e0

GenotypeDepth
all individuals: 30
bin: 9.75e1
variant carriers: 7

GenotypeDepth
all individuals: 32
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1359
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 150
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1147
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 238
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4202
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 12
allele frequency: 7.453416149068323e-3
allele num: 1610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.785714285714286e-3
allele num: 4480
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.89e-2

QD
type: SiteQuality
SIO_000300: 1.333e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.93e-1

DP
type: SiteQuality
SIO_000300: 2.2963e5

VQSLOD
type: SiteQuality
SIO_000300: 2.66e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 1.186e0

MQRankSum
type: SiteQuality
SIO_000300: 5.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

GenotypeDepth
all individuals: 2735
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 150
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 130
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4172
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 1.445086705202312e-3
allele num: 7612
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.888e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e0

MQ
type: SiteQuality
SIO_000300: 5.868e1

MQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

QD
type: SiteQuality
SIO_000300: 1.205e1

VQSLOD
type: SiteQuality
SIO_000300: 9.299999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.36e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

DP
type: SiteQuality
SIO_000300: 2.28358e5

GenotypeDepth
all individuals: 150
bin: 6.25e1
variant carriers: 122

GenotypeDepth
all individuals: 113
bin: 6.75e1
variant carriers: 99

GenotypeQuality
all individuals: 1112
bin: 7.5e0
variant carriers: 21

GenotypeQuality
all individuals: 482
bin: 2.25e1
variant carriers: 11

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 9

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3917
bin: 6.25e1
variant carriers: 13

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 213
bin: 7.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1964
bin: 9.75e1
variant carriers: 1547

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 9

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 11

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 10

GenotypeQuality
all individuals: 622
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 251
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 8

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 207
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 6

GenotypeQuality
all individuals: 146
bin: 8.25e1
variant carriers: 10

GenotypeQuality
all individuals: 74
bin: 8.75e1
variant carriers: 8

European (Non-Finnish)
type: Population
allele count: 616
allele frequency: 1.403828623518687e-1
allele num: 4388
num of homozygotes: 45

African
type: Population
allele count: 111
allele frequency: 1.585714285714286e-1
allele num: 700
num of homozygotes: 7

South Asian
type: Population
allele count: 743
allele frequency: 9.791776489193463e-2
allele num: 7588
num of homozygotes: 45

Other
type: Population
allele count: 20
allele frequency: 1.075268817204301e-1
allele num: 186
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 114
allele frequency: 7.107231920199501e-2
allele num: 1604
num of homozygotes: 4

East Asian
type: Population
allele count: 31
allele frequency: 1.565656565656566e-1
allele num: 198
num of homozygotes: 2

Latino
type: Population
allele count: 39
allele frequency: 2.010309278350516e-1
allele num: 194
num of homozygotes: 5

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.57e-2

QD
type: SiteQuality
SIO_000300: 1.378e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.236e0

MQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.44241e5

VQSLOD
type: SiteQuality
SIO_000300: 6.84e0

GenotypeDepth
all individuals: 9
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1492
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 9.75e1
variant carriers: 25

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3009
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 11
allele frequency: 1.476113794954375e-3
allele num: 7452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 578
num of homozygotes: 0

East Asian
type: Population
allele count: 12
allele frequency: 6.060606060606061e-2
allele num: 198
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 1.630434782608696e-2
allele num: 184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

QD
type: SiteQuality
SIO_000300: 1.622e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.03e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 1.81031e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.65e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

VQSLOD
type: SiteQuality
SIO_000300: 3.67e0