19-40745778-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745778
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745778
    reference: chr 19
allele count: 285
allele frequency: 1.299589603283174e-2
allele num: 21930
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+174C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+174C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2067C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+174C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+174C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+174C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1121C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+174C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+174C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-898C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+174C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+174C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+174C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+174C>T
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17340
  bin: 2.5e0
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29909
  bin: 7.5e0
  variant carriers: 194
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 2.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 1.25e1
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 2
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/19-40745782-A-ACC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745782
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745784
    reference: chr 19
allele count: 2
allele frequency: 8.106355382619974e-5
allele num: 24672
alternate allele: ACC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1115_1116dupGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+168_453+169dupGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-904_208-903dupGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+168_*253+169dupGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+168_967+169dupGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+168_*253+169dupGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+168_639+169dupGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+168_*253+169dupGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+168_639+169dupGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+168_104+169dupGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+168_639+169dupGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2061_74+2062dupGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+168_383+169dupGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+168_68+169dupGG
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14896
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-40745785-CCCA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745785
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745782
    reference: chr 19
allele count: 1
allele frequency: 3.706174486694834e-5
allele num: 26982
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+164_383+166delTGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+164_639+166delTGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+164_*253+166delTGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+164_639+166delTGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+164_68+166delTGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+164_*253+166delTGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1111_1113delTGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-908_208-906delTGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+164_104+166delTGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+164_967+166delTGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+164_453+166delTGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+164_639+166delTGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+164_*253+166delTGG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2057_74+2059delTGG
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: CCCA
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

19-40745792-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745792
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745790
    reference: chr 19
allele count: 7
allele frequency: 2.207923290436538e-4
allele num: 31704
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+158_453+159delAT
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1105_1106delAT
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+158_*253+159delAT
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-914_208-913delAT
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+158_639+159delAT
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+158_*253+159delAT
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+158_967+159delAT
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+158_639+159delAT
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+158_639+159delAT
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+158_*253+159delAT
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+158_104+159delAT
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+158_68+159delAT
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2051_74+2052delAT
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+158_383+159delAT
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32897
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10585
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7482
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: CAT
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-40745793-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745793
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745793
    reference: chr 19
allele count: 2
allele frequency: 6.169792694965449e-5
allele num: 32416
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1106T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+159T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+159T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+159T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+159T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-913T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+159T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+159T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+159T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+159T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+159T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+159T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+159T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2052T>C
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33052
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

19-40745799-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745799
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745799
    reference: chr 19
allele count: 1
allele frequency: 2.761058037439947e-5
allele num: 36218
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+153A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+153A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+153A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2046A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+153A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1100A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+153A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+153A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+153A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+153A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+153A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-919A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+153A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+153A>G
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8421
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-40745802-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745802
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745802
    reference: chr 19
allele count: 1
allele frequency: 2.587991718426501e-5
allele num: 38640
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+150A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2043A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+150A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1097A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+150A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-922A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+150A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+150A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+150A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+150A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+150A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+150A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+150A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+150A>G
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32748
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10053
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

19-40745804-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745804
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745804
    reference: chr 19
allele count: 1
allele frequency: 2.461356699812937e-5
allele num: 40628
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+148G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2041G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+148G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+148G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-924G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+148G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+148G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+148G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+148G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+148G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+148G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1095G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+148G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+148G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6869
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP

19-40745813-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745813
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745813
    reference: chr 19
allele count: 1
allele frequency: 1.83123351889833e-5
allele num: 54608
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1086A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+139A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+139A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+139A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+139A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+139A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+139A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+139A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+139A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-933A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+139A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+139A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2032A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+139A>G
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28419
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

19-40745815-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745815
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745815
    reference: chr 19
allele count: 1
allele frequency: 1.768033946251768e-5
allele num: 56560
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+137C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+137C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+137C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-935C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+137C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+137C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+137C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+137C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+137C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+137C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+137C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1084C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2030C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+137C>T
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-40745821-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745821
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745821
    reference: chr 19
allele count: 1
allele frequency: 1.51285930408472e-5
allele num: 66100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+131G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2024G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1078G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-941G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+131G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+131G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+131G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+131G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+131G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+131G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+131G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+131G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+131G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+131G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP

19-40745822-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745822
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745822
    reference: chr 19
allele count: 1
allele frequency: 1.429306500485964e-5
allele num: 69964
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+130C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+130C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1077C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+130C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+130C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-942C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+130C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+130C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+130C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+130C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+130C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+130C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+130C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2023C>T
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22205
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

19-40745829-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745829
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745829
    reference: chr 19
allele count: 1
allele frequency: 1.174287794452664e-5
allele num: 85158
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+123G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+123G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2016G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+123G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+123G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+123G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+123G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+123G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+123G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1070G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-949G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+123G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+123G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+123G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-40745831-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745831
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745831
    reference: chr 19
allele count: 1
allele frequency: 1.139497253811618e-5
allele num: 87758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+121G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+121G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+121G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2014G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-951G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+121G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1068G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+121G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+121G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+121G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+121G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+121G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+121G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+121G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31192
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14994
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

19-40745833-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745833
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745833
    reference: chr 19
allele count: 2
allele frequency: 2.221679145097865e-5
allele num: 90022
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+119A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+119A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+119A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+119A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1066A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+119A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+119A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+119A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+119A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-953A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+119A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+119A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+119A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2012A>G
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14072
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5874
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

19-40745843-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745843
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745843
    reference: chr 19
allele count: 5
allele frequency: 4.875290079759746e-5
allele num: 102558
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+109G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+109G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2002G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+109G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+109G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+109G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+109G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-963G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1056G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+109G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+109G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+109G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+109G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+109G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36509
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

19-40745844-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745844
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745844
    reference: chr 19
allele count: 1
allele frequency: 9.547815459822792e-6
allele num: 104736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-964C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+108C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2001C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1055C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+108C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+108C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+108C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+108C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+108C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+108C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+108C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+108C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+108C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+108C>T
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

19-40745844-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745844
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745844
    reference: chr 19
allele count: 1
allele frequency: 9.547815459822792e-6
allele num: 104736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+108C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+2001C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+108C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+108C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+108C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1055C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+108C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+108C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+108C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+108C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+108C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-964C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+108C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+108C>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP

19-40745874-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745874
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745874
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 118632
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+78G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+78G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+78G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1971G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+78G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+78G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1025G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-994G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+78G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+78G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+78G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+78G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+78G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+78G>C
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

19-40745880-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745880
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745880
    reference: chr 19
allele count: 1
allele frequency: 8.364001338240215e-6
allele num: 119560
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+72C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+72C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+72C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+72C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1019C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1000C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1965C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+72C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+72C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+72C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+72C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+72C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+72C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+72C>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

19-40745885-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745885
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745885
    reference: chr 19
allele count: 81
allele frequency: 6.742358660185124e-4
allele num: 120136
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+67C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+67C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+67C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+67C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1014C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+67C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+67C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+67C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+67C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+67C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1960C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+67C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1005C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+67C>G
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 43008
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10297
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

19-40745887-G-GCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745887
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745889
    reference: chr 19
allele count: 1
allele frequency: 8.313657676831499e-6
allele num: 120284
alternate allele: GCT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+63_104+64dupAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+63_453+64dupAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1956_74+1957dupAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+63_383+64dupAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+63_639+64dupAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+63_967+64dupAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+63_639+64dupAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1009_208-1008dupAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1010_1011dupAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+63_68+64dupAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+63_*253+64dupAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+63_*253+64dupAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+63_*253+64dupAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+63_639+64dupAG
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

19-40745887-GCT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745887
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745885
    reference: chr 19
allele count: 2
allele frequency: 1.6627315353663e-5
allele num: 120284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1010_1011delAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+63_104+64delAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+63_967+64delAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+63_*253+64delAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+63_383+64delAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+63_639+64delAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+63_*253+64delAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1956_74+1957delAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+63_639+64delAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+63_453+64delAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+63_639+64delAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+63_68+64delAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+63_*253+64delAG
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1009_208-1008delAG
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: GCT
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-40745887-GCTCT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745887
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745883
    reference: chr 19
allele count: 6
allele frequency: 4.988194606098899e-5
allele num: 120284
alternate allele: G
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43002
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3111
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2576
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7557
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41559
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2211
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 16498
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11528
  num of homozygotes: 0
population: African
  type: Population
  allele count: 6
  allele frequency: 5.881199764752009e-4
  allele num: 10202
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 902
  num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: GCTCT
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-40745893-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745893
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745893
    reference: chr 19
allele count: 1
allele frequency: 8.290361625574107e-6
allele num: 120622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1013A>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+59A>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1006A>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1952A>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+59A>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+59A>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+59A>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+59A>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+59A>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+59A>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+59A>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+59A>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+59A>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+59A>T
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5007
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

19-40745896-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745896
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745896
    reference: chr 19
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+56G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+56G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+56G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1016G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1949G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1003G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+56G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+56G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+56G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+56G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+56G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+56G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+56G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+56G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

19-40745899-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745899
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745899
    reference: chr 19
allele count: 1
allele frequency: 8.273899157717065e-6
allele num: 120862
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.1000T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+53T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+53T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+53T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+53T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+53T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+53T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1946T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+53T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+53T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1019T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+53T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+53T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+53T>C
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

19-40745901-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745901
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745901
    reference: chr 19
allele count: 2
allele frequency: 1.653849334325643e-5
allele num: 120930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+51G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+51G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+51G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+51G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1021G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+51G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+51G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+51G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+51G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.998G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+51G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1944G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+51G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+51G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

19-40745906-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745906
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745906
    reference: chr 19
allele count: 40
allele frequency: 3.304911097891467e-4
allele num: 121032
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1939A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.993A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+46A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+46A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+46A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+46A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+46A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+46A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+46A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+46A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+46A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+46A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1026A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+46A>G
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

19-40745914-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745914
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745914
    reference: chr 19
allele count: 4
allele frequency: 3.301365114474835e-5
allele num: 121162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1034G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+38G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+38G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+38G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1931G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+38G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.985G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+38G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+38G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+38G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+38G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+38G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+38G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+38G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum

19-40745919-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745919
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745919
    reference: chr 19
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+33G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.980G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1926G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1039G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+33G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+33G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+33G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+33G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+33G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+33G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+33G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+33G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+33G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+33G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

19-40745923-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745923
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745923
    reference: chr 19
allele count: 220
allele frequency: 1.814702388808235e-3
allele num: 121232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.976G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1922G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+29G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1043G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+29G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+29G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+29G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+29G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+29G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+29G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+29G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+29G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+29G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+29G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5059
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.75e1
  variant carriers: 183
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

19-40745926-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745926
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745926
    reference: chr 19
allele count: 3
allele frequency: 2.474349246148263e-5
allele num: 121244
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+26A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+26A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+26A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+26A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+26A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+26A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+26A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.973A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+26A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+26A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1046A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+26A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+26A>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1919A>G
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10525
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

19-40745927-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745927
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745927
    reference: chr 19
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+25C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+25C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+25C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+25C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1047C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+25C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1918C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+25C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+25C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+25C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+25C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.972C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+25C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+25C>T
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

19-40745933-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745933
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745933
    reference: chr 19
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1912C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.966C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.68+19C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*253+19C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*253+19C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1053C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.453+19C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.383+19C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*253+19C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.639+19C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.639+19C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.639+19C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.967+19C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.104+19C>T
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

19-40745961-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745961
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745961
    reference: chr 19
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1884G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.630G>A
  hgvsp: ENST00000392038.2:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*244G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*244G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.95G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.444G>A
  hgvsp: ENST00000579047.1:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.630G>A
  hgvsp: ENST00000424901.1:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.958G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.938G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.374G>A
  hgvsp: ENSP00000472371.1:p.Arg125His
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.630G>A
  hgvsp: ENST00000311278.6:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*244G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1081G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.59G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10560
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg125His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ

19-40745968-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745968
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745968
    reference: chr 19
allele count: 35
allele frequency: 2.884456897972639e-4
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*237G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.88G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.623G>A
  hgvsp: ENSP00000375892.2:p.Arg208Lys
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.951G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1877G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.437G>A
  hgvsp: ENSP00000471369.1:p.Arg146Lys
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.623G>A
  hgvsp: ENSP00000309428.6:p.Arg208Lys
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.367G>A
  hgvsp: ENSP00000472371.1:p.Gly123Ser
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.52G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*237G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.623G>A
  hgvsp: ENSP00000399532.1:p.Arg208Lys
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.931G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1088G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*237G>A
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg208Lys
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

19-40745971-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745971
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745971
    reference: chr 19
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.928C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.620C>G
  hgvsp: ENSP00000375892.2:p.Thr207Ser
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1874C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*234C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.85C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.364C>G
  hgvsp: ENSP00000472371.1:p.Pro122Ala
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.620C>G
  hgvsp: ENSP00000309428.6:p.Thr207Ser
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*234C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.434C>G
  hgvsp: ENSP00000471369.1:p.Thr145Ser
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.948C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1091C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.620C>G
  hgvsp: ENSP00000399532.1:p.Thr207Ser
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.49C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*234C>G
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr207Ser
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

19-40745985-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745985
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745985
    reference: chr 19
allele count: 16
allele frequency: 1.318500206015657e-4
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.606G>A
  hgvsp: ENST00000392038.2:c.606G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.420G>A
  hgvsp: ENST00000579047.1:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.71G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.606G>A
  hgvsp: ENST00000311278.6:c.606G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.606G>A
  hgvsp: ENST00000424901.1:c.606G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.934G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1105G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.350G>A
  hgvsp: ENSP00000472371.1:p.Gly117Glu
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*220G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.914G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*220G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*220G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1860G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.35G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*411G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
hgvs: p.Gly117Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

19-40745987-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745987
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745987
    reference: chr 19
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*218C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.604C>T
  hgvsp: ENSP00000309428.6:p.Arg202Trp
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.418C>T
  hgvsp: ENSP00000471369.1:p.Arg140Trp
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*409C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.912C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.348C>T
  hgvsp: ENST00000601166.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.33C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.932C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.604C>T
  hgvsp: ENSP00000375892.2:p.Arg202Trp
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.69C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*218C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.604C>T
  hgvsp: ENSP00000399532.1:p.Arg202Trp
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*218C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1858C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1107C>T
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg202Trp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

19-40745994-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745994
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745994
    reference: chr 19
allele count: 49
allele frequency: 4.038039984836748e-4
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1114C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.26C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.597C>T
  hgvsp: ENST00000392038.2:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.597C>T
  hgvsp: ENST00000424901.1:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1851C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.341C>T
  hgvsp: ENSP00000472371.1:p.Pro114Leu
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*211C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*211C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.597C>T
  hgvsp: ENST00000311278.6:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.905C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.411C>T
  hgvsp: ENST00000579047.1:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.925C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*211C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*402C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.62C>T
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro114Leu
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

19-40745999-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40745999
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40745999
    reference: chr 19
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*206G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*206G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*397G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.336G>A
  hgvsp: ENST00000601166.1:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.592G>A
  hgvsp: ENSP00000309428.6:p.Val198Ile
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*206G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.592G>A
  hgvsp: ENSP00000399532.1:p.Val198Ile
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.592G>A
  hgvsp: ENSP00000375892.2:p.Val198Ile
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.406G>A
  hgvsp: ENSP00000471369.1:p.Val136Ile
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.920G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1846G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1119G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.900G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.21G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.57G>A
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val198Ile
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum

19-40746008-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746008
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746008
    reference: chr 19
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*388G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1837G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.327G>A
  hgvsp: ENST00000601166.1:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.12G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1128G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.48G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.583G>A
  hgvsp: ENSP00000375892.2:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.891G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.911G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.397G>A
  hgvsp: ENSP00000471369.1:p.Ala133Thr
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*197G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.583G>A
  hgvsp: ENSP00000309428.6:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*197G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*197G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.583G>A
  hgvsp: ENSP00000399532.1:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala195Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-40746009-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746009
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746009
    reference: chr 19
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*196C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.890C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.582C>T
  hgvsp: ENST00000311278.6:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.47C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*196C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.326C>T
  hgvsp: ENSP00000472371.1:p.Ser109Leu
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.582C>T
  hgvsp: ENST00000424901.1:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.396C>T
  hgvsp: ENST00000579047.1:c.396C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.11C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1129C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.582C>T
  hgvsp: ENST00000392038.2:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*387C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1836C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*196C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.910C>T
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser109Leu
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: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-40746015-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746015
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746015
    reference: chr 19
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.576T>G
  hgvsp: ENSP00000399532.1:p.Asp192Glu
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1830T>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*190T>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*190T>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*381T>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.576T>G
  hgvsp: ENSP00000375892.2:p.Asp192Glu
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.576T>G
  hgvsp: ENSP00000309428.6:p.Asp192Glu
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.390T>G
  hgvsp: ENSP00000471369.1:p.Asp130Glu
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.320T>G
  hgvsp: ENSP00000472371.1:p.Met107Arg
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.904T>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.5T>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.884T>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1135T>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.41T>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*190T>G
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42945
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp192Glu
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-40746032-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746032
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746032
    reference: chr 19
allele count: 18
allele frequency: 1.483679525222552e-4
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-15G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-15G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-15G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-15G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.39-15G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-15G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1813G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1152G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-15G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-15G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-15G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-4G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-15G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-15G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-15G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.307-4G>A
num of homozygotes: 1
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

19-40746033-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746033
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746033
    reference: chr 19
allele count: 2
allele frequency: 1.648505629646725e-5
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-16C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-16C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-16C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-16C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.39-16C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-16C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-16C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-16C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-5C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-16C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-16C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1153C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-16C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-16C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1812C>T
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.307-5C>T
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-40746033-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746033
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746033
    reference: chr 19
allele count: 9
allele frequency: 7.418275333410263e-5
allele num: 121322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-16C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-5C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-16C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-16C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-16C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-16C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-16C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-16C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1812C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-16C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-16C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-16C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1153C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-16C>G
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.39-16C>G
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
hgvs: c.307-5C>G
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

19-40746034-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746034
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746034
    reference: chr 19
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-17C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-17C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-17C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-6C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-17C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-17C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-17C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1154C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1811C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-17C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.39-17C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-17C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-17C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-17C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-17C>T
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10561
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.307-6C>T
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-40746034-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746034
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746034
    reference: chr 19
allele count: 4
allele frequency: 3.297174321606383e-5
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-17C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-17C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1811C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-17C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-6C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.39-17C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-17C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-17C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-17C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-17C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-17C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-17C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-17C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1154C>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-17C>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.307-6C>A
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

19-40746038-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746038
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746037
    reference: chr 19
allele count: 20
allele frequency: 1.648614339647526e-4
allele num: 121314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-22delC
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1159delC
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-22delC
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-11delC
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-22delC
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-22delC
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-22delC
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-22delC
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-22delC
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-22delC
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.39-22delC
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-22delC
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-22delC
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-22delC
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1806delC
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: AG
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

19-40746050-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746050
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746050
    reference: chr 19
allele count: 2
allele frequency: 1.64883180266781e-5
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-33C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-33C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1170C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.39-33C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-33C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1795C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-33C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-33C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-33C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-33C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-22C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-33C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-33C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-33C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-33C>T
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

19-40746064-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746064
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746064
    reference: chr 19
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-47C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-47C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-47C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-47C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.39-47C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1184C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-47C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-47C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-36C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-47C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-47C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-47C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-47C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1781C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-47C>T
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

19-40746072-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746072
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746072
    reference: chr 19
allele count: 6
allele frequency: 4.948371985616732e-5
allele num: 121252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-55G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-55G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-55G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1773G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-44G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-55G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1192G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.39-55G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-55G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-55G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-55G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-55G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-55G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-55G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-55G>A
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10478
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-40746073-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746073
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746073
    reference: chr 19
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-56C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-56C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-56C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-45C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1193C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-56C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-56C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-56C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.39-56C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-56C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-56C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-56C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1772C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-56C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-56C>T
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

19-40746076-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746076
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746076
    reference: chr 19
allele count: 4
allele frequency: 3.298914657077821e-5
allele num: 121252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1769G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-59G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-59G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-59G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-59G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-59G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-59G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-59G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-59G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-59G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.39-59G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-48G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1196G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-59G>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-59G>C
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

19-40746077-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746077
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746077
    reference: chr 19
allele count: 3
allele frequency: 2.474512521033356e-5
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1197G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-60G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-60G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1768G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-60G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-60G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-49G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-60G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-60G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-60G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-60G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-60G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.39-60G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-60G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-60G>A
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

19-40746078-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746078
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746078
    reference: chr 19
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1198C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-50C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-61C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-61C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-61C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-61C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-61C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-61C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-61C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1767C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-61C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-61C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-61C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.39-61C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-61C>T
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10522
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

19-40746123-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746123
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746123
    reference: chr 19
allele count: 4
allele frequency: 3.372624407682838e-5
allele num: 118602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-106G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-106G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-106G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-106G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-95G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-106G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-106G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-106G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-106G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-106G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-106G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.38+46G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1722G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-106G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1243G>A
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

19-40746137-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746137
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746136
    reference: chr 19
allele count: 1
allele frequency: 8.500365515717176e-6
allele num: 117642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-110delA
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-121delA
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-121delA
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-121delA
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-121delA
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-121delA
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.38+31delA
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1707delA
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1258delA
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-121delA
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-121delA
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-121delA
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-121delA
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-121delA
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-121delA
  variant of: http://identifiers.org/hgnc/392
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: AT
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

19-40746167-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746167
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746167
    reference: chr 19
allele count: 1
allele frequency: 9.26509283623022e-6
allele num: 107932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-150T>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.38+2T>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1678T>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-150T>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-150T>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-150T>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-139T>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-150T>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-150T>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1287T>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-150T>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-150T>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-150T>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-150T>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-150T>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.38+2T>A
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: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

19-40746170-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746170
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746170
    reference: chr 19
allele count: 1
allele frequency: 9.390376741914886e-6
allele num: 106492
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1290G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-153G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.37G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-153G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-153G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-153G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1675G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-153G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-142G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-153G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-153G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-153G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-153G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-153G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-153G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.37G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

19-40746192-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746192
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746192
    reference: chr 19
allele count: 15
allele frequency: 1.801758516311921e-4
allele num: 83252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1653G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-175G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-175G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1312G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.15G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-175G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-175G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-175G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-175G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-175G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-175G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-175G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-175G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-164G>A
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-175G>A
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9912
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14764
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6123
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 1.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

19-40746193-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746193
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746193
    reference: chr 19
allele count: 2
allele frequency: 2.411498022571622e-5
allele num: 82936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-176C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.14C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-176C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-176C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-176C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-176C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-176C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-176C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-165C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-176C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-176C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-176C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1652C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1313C>T
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-176C>T
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14839
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13966
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9887
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

19-40746194-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 40746194
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 40746194
    reference: chr 19
allele count: 2
allele frequency: 2.457787499692777e-5
allele num: 81374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000480878
  gene symbol: AKT2
  hgvsc: ENST00000480878.2:n.3-177T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000476266
  gene symbol: AKT2
  hgvsc: ENST00000476266.1:n.902-177T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462469
  ensembl transcript: ENST00000584288
  gene symbol: AKT2
  hgvsc: ENST00000584288.1:c.*188-177T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000472371
  ensembl transcript: ENST00000601166
  gene symbol: AKT2
  hgvsc: ENST00000601166.1:c.307-166T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000391845
  gene symbol: AKT2
  hgvsc: ENST00000391845.2:n.13T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000471369
  ensembl transcript: ENST00000579047
  gene symbol: AKT2
  hgvsc: ENST00000579047.1:c.388-177T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375892
  ensembl transcript: ENST00000392038
  gene symbol: AKT2
  hgvsc: ENST00000392038.2:c.574-177T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl transcript: ENST00000537834
  gene symbol: AKT2
  hgvsc: ENST00000537834.1:n.882-177T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462776
  ensembl transcript: ENST00000492463
  gene symbol: AKT2
  hgvsc: ENST00000492463.2:c.*188-177T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000375719
  ensembl transcript: ENST00000391844
  gene symbol: AKT2
  hgvsc: ENST00000391844.4:c.*188-177T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000309428
  ensembl transcript: ENST00000311278
  gene symbol: AKT2
  hgvsc: ENST00000311278.6:c.574-177T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000399532
  ensembl transcript: ENST00000424901
  gene symbol: AKT2
  hgvsc: ENST00000424901.1:c.574-177T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000462919
  ensembl transcript: ENST00000578310
  gene symbol: AKT2
  hgvsc: ENST00000578310.1:c.74+1651T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463262
  ensembl transcript: ENST00000578615
  gene symbol: AKT2
  hgvsc: ENST00000578615.1:c.208-1314T>C
  variant of: http://identifiers.org/hgnc/392
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105221
  ensembl protein: ENSP00000463086
  ensembl transcript: ENST00000491778
  gene symbol: AKT2
  hgvsc: ENST00000491778.2:c.*379-177T>C
  variant of: http://identifiers.org/hgnc/392
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14501
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4542
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1410
bin: 2.75e1
variant carriers: 3

GenotypeDepth
all individuals: 38
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 192
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16757
bin: 7.5e0
variant carriers: 7

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 8

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 8

GenotypeQuality
all individuals: 397
bin: 7.75e1
variant carriers: 16

GenotypeQuality
all individuals: 5154
bin: 6.25e1
variant carriers: 14

GenotypeQuality
all individuals: 989
bin: 3.25e1
variant carriers: 14

GenotypeQuality
all individuals: 1003
bin: 6.75e1
variant carriers: 17

GenotypeQuality
all individuals: 131
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 486
bin: 9.75e1
variant carriers: 323

GenotypeQuality
all individuals: 416
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 149
bin: 8.75e1
variant carriers: 13

GenotypeQuality
all individuals: 412
bin: 7.25e1
variant carriers: 12

GenotypeQuality
all individuals: 870
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 12

GenotypeQuality
all individuals: 979
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1152
bin: 2.75e1
variant carriers: 10

GenotypeQuality
all individuals: 27719
bin: 2.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1335
bin: 1.75e1
variant carriers: 9

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 308
bin: 8.25e1
variant carriers: 21

African
type: Population
allele count: 1
allele frequency: 7.541478129713424e-4
allele num: 1326
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 1.851851851851852e-2
allele num: 216
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.103752759381898e-4
allele num: 9060
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 136
allele frequency: 1.505423953951738e-2
allele num: 9034
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.724795640326975e-3
allele num: 734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 141
allele frequency: 1.784810126582279e-1
allele num: 790
num of homozygotes: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.718e0

VQSLOD
type: SiteQuality
SIO_000300: 5.88e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.03e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 4.99898e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.353e1

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

GenotypeDepth
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5597
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1038
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14391
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29555
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1304
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1354
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5696
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1511
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.140410958904109e-4
allele num: 9344
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 970
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 922
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10752
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -6.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.45e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.12e-2

QD
type: SiteQuality
SIO_000300: 1.395e1

DP
type: SiteQuality
SIO_000300: 5.28862e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32036
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 187
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1474
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30303
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12935
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6145
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 793
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 428
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1022
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 3.846153846153846e-3
allele num: 260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1102
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1048
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1772
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12186
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.404e0

VQSLOD
type: SiteQuality
SIO_000300: 8.9e-2

MQ
type: SiteQuality
SIO_000300: 5.604e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.82e-2

DP
type: SiteQuality
SIO_000300: 5.50577e5

QD
type: SiteQuality
SIO_000300: 2.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.25e-1

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 187
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10277
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1697
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7365
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31362
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 144
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1724
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 456
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1197
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1288
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 3.302073702285035e-4
allele num: 15142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1384
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 296
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.995211492418196e-4
allele num: 10024
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.03e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.728e1

DP
type: SiteQuality
SIO_000300: 5.94388e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.32e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

GenotypeDepth
all individuals: 46
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 195
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7722
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 187
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1732
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9902
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7590
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 305
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1743
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31634
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1215
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.485884101040119e-3
allele num: 1346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1422
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2252
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.28e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.166e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 6.00234e5

QD
type: SiteQuality
SIO_000300: 1.33e1

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4887
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1792
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1857
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8696
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8178
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31709
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 3.75e1
variant carriers: 0

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

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

South Asian
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European (Non-Finnish)
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Latino
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African
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Other
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European (Finnish)
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DP
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QD
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BaseQRankSum
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MQ
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Finnish)
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East Asian
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European (Non-Finnish)
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African
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South Asian
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Latino
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ReadPosRankSum
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QD
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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ClippingRankSum
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DP
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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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African
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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QD
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InbreedingCoeff
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FS
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MQ
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DP
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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bin: 7.75e1
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46998
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 1.528117359413203e-4
allele num: 6544
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele num: 49518
num of homozygotes: 0

Latino
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East Asian
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South Asian
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ReadPosRankSum
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VQSLOD
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MQ
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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MQRankSum
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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 frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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African
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South Asian
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Other
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Latino
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East Asian
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DP
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ClippingRankSum
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FS
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MQ
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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InbreedingCoeff
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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African
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allele num: 8352
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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num of homozygotes: 0

East Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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African
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Latino
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MQRankSum
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BaseQRankSum
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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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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bin: 9.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64870
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

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

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

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

ClippingRankSum
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SIO_000300: -2.15e-1

ReadPosRankSum
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SIO_000300: 3.1e-2

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 1.51e0

VQSLOD
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SIO_000300: 2.25e-1

DP
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SIO_000300: 1.41766e6

MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 1.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
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SIO_000300: 1.272e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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bin: 9.25e1
variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65500
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
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SIO_000300: 1.427968e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
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SIO_000300: 4.2e0

QD
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SIO_000300: 1.273e1

ReadPosRankSum
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SIO_000300: 8.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.08e-1

BaseQRankSum
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SIO_000300: -5.152e0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 7

GenotypeDepth
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GenotypeDepth
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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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variant carriers: 81

GenotypeQuality
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variant carriers: 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: 3
allele frequency: 4.553181155900923e-5
allele num: 65888
num of homozygotes: 0

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

African
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allele count: 70
allele frequency: 6.887052341597796e-3
allele num: 10164
num of homozygotes: 0

Latino
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allele count: 7
allele frequency: 6.075334143377885e-4
allele num: 11522
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.5e-3

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -2.571e0

MQ
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SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-2

ReadPosRankSum
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SIO_000300: 3.35e-1

MQRankSum
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SIO_000300: 6.7e-2

QD
type: SiteQuality
SIO_000300: 1.561e1

VQSLOD
type: SiteQuality
SIO_000300: 4.96e0

DP
type: SiteQuality
SIO_000300: 1.438063e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 65964
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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DP
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SIO_000300: 1.441195e6

QD
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ReadPosRankSum
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SIO_000300: 5.53e-1

InbreedingCoeff
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FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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SIO_000300: 6.65e-1

VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.61e-1

MQ
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SIO_000300: 5.765e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Latino
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allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele num: 16498
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African
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European (Non-Finnish)
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allele frequency: 1.515978412467406e-5
allele num: 65964
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BaseQRankSum
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MQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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FS
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DP
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QD
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InbreedingCoeff
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ClippingRankSum
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65964
num of homozygotes: 0

East Asian
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MQ
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QD
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FS
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MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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num of homozygotes: 0

South Asian
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Latino
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Other
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.510528382828313e-5
allele num: 66202
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508659706716553e-5
allele num: 66284
num of homozygotes: 0

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

European (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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ReadPosRankSum
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MQRankSum
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MQ
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FS
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ClippingRankSum
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QD
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DP
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BaseQRankSum
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SIO_000300: -4.512e0

VQSLOD
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InbreedingCoeff
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SIO_000300: -4.0e-4

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

African
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allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.656509695290859e-5
allele num: 11552
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 902
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66352
num of homozygotes: 0

South Asian
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VQSLOD
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ReadPosRankSum
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MQRankSum
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MQ
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BaseQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

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

South Asian
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allele frequency: 1.211680600993578e-4
allele num: 16506
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66398
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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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

BaseQRankSum
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SIO_000300: -5.896e0

MQ
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SIO_000300: 5.948e1

QD
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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SIO_000300: 1.02e-1

ReadPosRankSum
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SIO_000300: 4.91e-1

FS
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SIO_000300: 8.84e-1

MQRankSum
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DP
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SIO_000300: 1.448965e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 40

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 38
allele frequency: 5.716692742809002e-4
allele num: 66472
num of homozygotes: 0

European (Finnish)
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allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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MQ
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: -7.0e-4

FS
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DP
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SIO_000300: 1.45399e6

QD
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GenotypeDepth
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variant carriers: 0

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

Latino
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European (Non-Finnish)
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South Asian
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East Asian
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African
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Other
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DP
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MQ
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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QD
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Latino
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allele num: 11572
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European (Non-Finnish)
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allele frequency: 3.048048048048048e-3
allele num: 66600
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Other
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East Asian
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European (Finnish)
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allele num: 6614
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African
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South Asian
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ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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DP
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MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeDepth
all individuals: 81
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 835
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2630
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7666
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1115
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 41812
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 992
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

FS
type: SiteQuality
SIO_000300: 2.486e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.483227e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.54e-1

QD
type: SiteQuality
SIO_000300: 1.571e1

GenotypeDepth
all individuals: 12
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 58
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variant carriers: 0

GenotypeDepth
all individuals: 80
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variant carriers: 0

GenotypeDepth
all individuals: 43077
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variant carriers: 0

GenotypeDepth
all individuals: 241
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variant carriers: 1

GenotypeDepth
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 7669
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 85
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2235
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3153
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 9.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.14e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.357e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.71e-1

FS
type: SiteQuality
SIO_000300: 1.2143e1

DP
type: SiteQuality
SIO_000300: 1.483247e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.319e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

QD
type: SiteQuality
SIO_000300: 1.928e1

GenotypeDepth
all individuals: 22
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 73
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variant carriers: 0

GenotypeDepth
all individuals: 8
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 17
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

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

GenotypeQuality
all individuals: 990
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variant carriers: 0

GenotypeQuality
all individuals: 3156
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2629
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variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2236
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variant carriers: 0

GenotypeQuality
all individuals: 1118
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variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.25e1
variant carriers: 0

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

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

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

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: 10386
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.362e0

MQRankSum
type: SiteQuality
SIO_000300: -1.66e-1

MQ
type: SiteQuality
SIO_000300: 5.99e1

QD
type: SiteQuality
SIO_000300: 1.239e1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e-1

FS
type: SiteQuality
SIO_000300: 7.7e-1

DP
type: SiteQuality
SIO_000300: 1.483568e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.346e0

GenotypeDepth
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 243
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variant carriers: 1

GenotypeDepth
all individuals: 28
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variant carriers: 0

GenotypeDepth
all individuals: 77
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variant carriers: 0

GenotypeDepth
all individuals: 5072
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variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 1121
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variant carriers: 1

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

GenotypeQuality
all individuals: 2633
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 2234
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3159
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 992
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variant carriers: 0

GenotypeQuality
all individuals: 933
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variant carriers: 0

GenotypeQuality
all individuals: 7672
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

MQRankSum
type: SiteQuality
SIO_000300: -2.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.919e0

DP
type: SiteQuality
SIO_000300: 1.48469e6

QD
type: SiteQuality
SIO_000300: 1.209e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.39e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

GenotypeDepth
all individuals: 43046
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 179
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variant carriers: 0

GenotypeDepth
all individuals: 273
bin: 9.75e1
variant carriers: 30

GenotypeDepth
all individuals: 839
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variant carriers: 0

GenotypeDepth
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 7675
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 41842
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 2235
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 3156
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 8
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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
all individuals: 1156
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variant carriers: 35

GenotypeQuality
all individuals: 2631
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
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 (Non-Finnish)
type: Population
allele count: 31
allele frequency: 4.649349091127242e-4
allele num: 66676
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.95e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 5.89e-1

QD
type: SiteQuality
SIO_000300: 1.3e1

VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

MQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.492053e6

GenotypeDepth
all individuals: 13
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
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variant carriers: 0

GenotypeDepth
all individuals: 10
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variant carriers: 0

GenotypeDepth
all individuals: 15
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
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GenotypeQuality
all individuals: 4
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3155
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

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

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

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 3.332e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.371e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 1.489111e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

QD
type: SiteQuality
SIO_000300: 1.441e1

VQSLOD
type: SiteQuality
SIO_000300: 4.11e-1

GenotypeDepth
all individuals: 13
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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
all individuals: 13
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GenotypeQuality
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GenotypeQuality
all individuals: 43
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GenotypeQuality
all individuals: 2631
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 9.689922480620155e-4
allele num: 16512
num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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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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allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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QD
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MQRankSum
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MQ
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FS
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DP
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 66682
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East Asian
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South Asian
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African
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Other
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European (Finnish)
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MQ
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SIO_000300: 5.929e1

BaseQRankSum
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FS
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VQSLOD
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DP
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Latino
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allele frequency: 6.909656244601831e-4
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66680
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East Asian
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South Asian
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African
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European (Finnish)
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allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
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African
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South Asian
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Other
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European (Finnish)
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East Asian
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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MQ
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VQSLOD
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QD
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InbreedingCoeff
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DP
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FS
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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European (Non-Finnish)
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African
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South Asian
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Other
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European (Finnish)
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FS
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VQSLOD
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InbreedingCoeff
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DP
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BaseQRankSum
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MQ
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MQRankSum
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QD
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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African
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East Asian
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Latino
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European (Non-Finnish)
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Other
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South Asian
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European (Finnish)
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BaseQRankSum
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QD
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InbreedingCoeff
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MQ
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VQSLOD
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FS
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ReadPosRankSum
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DP
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele num: 11578
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African
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European (Non-Finnish)
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MQ
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ReadPosRankSum
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FS
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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QD
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 6.046993780234969e-4
allele num: 11576
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South Asian
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European (Non-Finnish)
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allele num: 66662
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European (Finnish)
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East Asian
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Other
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InbreedingCoeff
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ReadPosRankSum
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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MQRankSum
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DP
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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African
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European (Non-Finnish)
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allele num: 66664
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Other
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Latino
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MQ
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BaseQRankSum
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MQRankSum
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FS
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DP
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QD
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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Other
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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Latino
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East Asian
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European (Finnish)
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QD
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BaseQRankSum
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MQRankSum
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FS
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MQ
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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African
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Other
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South Asian
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European (Non-Finnish)
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European (Finnish)
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East Asian
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InbreedingCoeff
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BaseQRankSum
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DP
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QD
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MQ
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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Latino
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European (Non-Finnish)
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South Asian
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QD
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MQ
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MQRankSum
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FS
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DP
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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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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variant carriers: 0

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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

East Asian
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allele frequency: 2.196531791907515e-3
allele num: 8650
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QD
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
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Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
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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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.5004651441947e-5
allele num: 66646
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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QD
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FS
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Other
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 1.50105073551486e-5
allele num: 66620
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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Other
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East Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 7.505704335294824e-5
allele num: 66616
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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num of homozygotes: 0

European (Non-Finnish)
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Latino
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South Asian
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African
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allele frequency: 9.632055480639569e-5
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European (Finnish)
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Other
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DP
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MQRankSum
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FS
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QD
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ReadPosRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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South Asian
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 6.005104338687885e-5
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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MQ
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QD
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FS
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ReadPosRankSum
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VQSLOD
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Finnish)
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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QD
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BaseQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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East Asian
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European (Non-Finnish)
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African
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Other
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FS
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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MQ
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VQSLOD
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QD
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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East Asian
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South Asian
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DP
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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Other
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South Asian
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MQRankSum
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QD
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FS
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InbreedingCoeff
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DP
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BaseQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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Latino
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African
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South Asian
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East Asian
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European (Finnish)
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VQSLOD
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MQ
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FS
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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DP
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Latino
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East Asian
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African
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European (Finnish)
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DP
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QD
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GenotypeQuality
all individuals: 2091
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.220347262311825e-5
allele num: 45038
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5320
num of homozygotes: 0

Latino
type: Population
allele count: 14
allele frequency: 2.125721226844823e-3
allele num: 6586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 656
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

DP
type: SiteQuality
SIO_000300: 1.204105e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.383e1

GenotypeDepth
all individuals: 407
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 824
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 565
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2179
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 692
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 648
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 112
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 208
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5721
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 436
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25083
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14560
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2040
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1945
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4400
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1748
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44858
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6220
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.14694110920526e-5
allele num: 13992
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5310
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.86706497386109e-4
allele num: 5356
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

DP
type: SiteQuality
SIO_000300: 1.200225e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.23e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.11e-1

QD
type: SiteQuality
SIO_000300: 1.669e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.82e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.01e-1

GenotypeDepth
all individuals: 646
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15485
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variant carriers: 0

GenotypeDepth
all individuals: 2119
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 270
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5683
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 564
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 692
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 648
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12970
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 333
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25971
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4709
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1856
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2085
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5721
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 844
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1898
bin: 6.75e1
variant carriers: 0