8-67710889-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67710889
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67710889
    reference: chr 8
allele count: 1
allele frequency: 8.323483877411729e-6
allele num: 120142
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.180+29T>A
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.180+29T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.180+29T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.180+29T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.180+29T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.180+29T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-22+29T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.180+29T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.510+29T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.180+29T>A
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

8-67710893-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67710893
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67710893
    reference: chr 8
allele count: 1
allele frequency: 8.325978718798394e-6
allele num: 120106
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.510+33A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.180+33A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-22+33A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.180+33A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.180+33A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.180+33A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.180+33A>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.180+33A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.180+33A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.180+33A>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5543
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4972
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6212
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

8-67710902-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67710902
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67710902
    reference: chr 8
allele count: 1
allele frequency: 8.365820603342981e-6
allele num: 119534
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.180+42C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.180+42C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.180+42C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.180+42C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-22+42C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.180+42C>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.180+42C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.510+42C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.180+42C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.180+42C>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6210
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1321
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

8-67710903-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67710903
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67710903
    reference: chr 8
allele count: 10
allele frequency: 8.364141253617491e-5
allele num: 119558
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.180+43C>T
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.180+43C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-22+43C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.180+43C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.180+43C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.180+43C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.180+43C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.180+43C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.180+43C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.510+43C>T
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum

8-67710904-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67710904
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67710904
    reference: chr 8
allele count: 3
allele frequency: 2.509998159334683e-5
allele num: 119522
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.180+44G>A
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.180+44G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.180+44G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.180+44G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-22+44G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.180+44G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.180+44G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.180+44G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.510+44G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.180+44G>A
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6211
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
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: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

8-67710906-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67710906
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67710907
    reference: chr 8
allele count: 1
allele frequency: 8.36638053645232e-6
allele num: 119526
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.180+50dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.180+50dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.510+50dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.180+50dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.180+50dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.180+50dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-22+50dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.180+50dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.180+50dupA
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.180+50dupA
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44930
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3182
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum

8-67710911-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67710911
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67710911
    reference: chr 8
allele count: 1
allele frequency: 8.377173876620983e-6
allele num: 119372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.180+51C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.180+51C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.180+51C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.180+51C>T
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-22+51C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.510+51C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.180+51C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.180+51C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.180+51C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.180+51C>T
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44930
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-67716559-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716559
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716559
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 79756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.181-51C>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.181-51C>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-21-51C>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.181-51C>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.181-51C>A
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.181-51C>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.181-51C>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.511-51C>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.181-51C>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.181-51C>A
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12964
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8858
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11921
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10547
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6014
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2366
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1960
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

8-67716560-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716560
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716560
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 80006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.181-50T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.511-50T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-21-50T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.181-50T>C
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.181-50T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.181-50T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.181-50T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.181-50T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.181-50T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.181-50T>C
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12958
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8856
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10534
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1789
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2670
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5750
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-67716562-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716562
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716562
    reference: chr 8
allele count: 4
allele frequency: 5.00462928208593e-5
allele num: 79926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.181-48G>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-21-48G>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.181-48G>T
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.181-48G>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.181-48G>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.181-48G>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.181-48G>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.181-48G>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.181-48G>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.511-48G>T
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8836
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10526
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10714
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8790
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12952
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5530
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1638
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6372
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ

8-67716570-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716570
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716569
    reference: chr 8
allele count: 6
allele frequency: 7.451194674879539e-5
allele num: 80524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.181-39delT
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.181-39delT
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.511-39delT
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.181-39delT
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.181-39delT
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-21-39delT
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.181-39delT
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.181-39delT
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.181-39delT
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.181-39delT
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14489
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11032
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12090
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8301
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5217
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12362
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9079
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: AT
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/8-67716572-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716572
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716572
    reference: chr 8
allele count: 6
allele frequency: 7.433470439565885e-5
allele num: 80716
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.181-38A>C
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.181-38A>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.181-38A>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.181-38A>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.181-38A>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-21-38A>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.181-38A>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.181-38A>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.181-38A>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.511-38A>C
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11444
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16051
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8015
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4289
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5048
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2847
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

8-67716578-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716578
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716578
    reference: chr 8
allele count: 1
allele frequency: 1.223540927444023e-5
allele num: 81730
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-21-32A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.181-32A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.181-32A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.181-32A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.181-32A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.511-32A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.181-32A>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.181-32A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.181-32A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.181-32A>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20442
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2963
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4079
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

8-67716584-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716584
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716584
    reference: chr 8
allele count: 1
allele frequency: 1.174480879451283e-5
allele num: 85144
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.181-26T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.181-26T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.511-26T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.181-26T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-21-26T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.181-26T>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.181-26T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.181-26T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.181-26T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.181-26T>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4373
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1447
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4118
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

8-67716586-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716586
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716586
    reference: chr 8
allele count: 1
allele frequency: 1.151596112211525e-5
allele num: 86836
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.181-24T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.511-24T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.181-24T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-21-24T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.181-24T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.181-24T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.181-24T>C
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.181-24T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.181-24T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.181-24T>C
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5957
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1864
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3370
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

8-67716592-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716592
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716592
    reference: chr 8
allele count: 1
allele frequency: 1.063467755657649e-5
allele num: 94032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.181-18T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.181-18T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.181-18T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.181-18T>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.181-18T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.181-18T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-21-18T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.181-18T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.511-18T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.181-18T>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11804
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-67716595-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716595
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716595
    reference: chr 8
allele count: 2
allele frequency: 2.049558320182001e-5
allele num: 97582
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-21-15T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.181-15T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.181-15T>C
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.181-15T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.181-15T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.181-15T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.181-15T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.181-15T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.181-15T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.511-15T>C
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6846
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32058
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP

8-67716604-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716604
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716604
    reference: chr 8
allele count: 1
allele frequency: 9.033423667570008e-6
allele num: 110700
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.511-6T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-21-6T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.181-6T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.181-6T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.181-6T>C
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.181-6T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.181-6T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.181-6T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.181-6T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.181-6T>C
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7537
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 2.75e1
  variant carriers: 0
hgvs: c.181-6T>C
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

8-67716611-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716611
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716611
    reference: chr 8
allele count: 1
allele frequency: 8.540293102859289e-6
allele num: 117092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.182T>A
  hgvsp: ENSP00000428972.1:p.Leu61Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-97T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.182T>A
  hgvsp: ENSP00000430256.1:p.Leu61Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.182T>A
  hgvsp: ENSP00000430463.1:p.Leu61Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.182T>A
  hgvsp: ENSP00000331816.5:p.Leu61Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.182T>A
  hgvsp: ENSP00000430691.1:p.Leu61Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.182T>A
  hgvsp: ENSP00000379842.1:p.Leu61Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-20T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.182T>A
  hgvsp: ENSP00000429606.1:p.Leu61Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.182T>A
  hgvsp: ENSP00000429022.1:p.Leu61Ter
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.512T>A
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu61Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

8-67716614-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716614
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716614
    reference: chr 8
allele count: 1
allele frequency: 8.454514710855598e-6
allele num: 118280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.185A>G
  hgvsp: ENSP00000429606.1:p.Lys62Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-17A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-94A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.185A>G
  hgvsp: ENSP00000429022.1:p.Lys62Arg
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.185A>G
  hgvsp: ENSP00000430256.1:p.Lys62Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.185A>G
  hgvsp: ENSP00000428972.1:p.Lys62Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.185A>G
  hgvsp: ENSP00000331816.5:p.Lys62Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.185A>G
  hgvsp: ENSP00000379842.1:p.Lys62Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.185A>G
  hgvsp: ENSP00000430463.1:p.Lys62Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.185A>G
  hgvsp: ENSP00000430691.1:p.Lys62Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.515A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.-17A>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys62Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

8-67716615-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716615
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716615
    reference: chr 8
allele count: 1
allele frequency: 8.436825053995681e-6
allele num: 118528
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.186A>G
  hgvsp: ENST00000522398.1:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.186A>G
  hgvsp: ENST00000520976.1:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-93A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.186A>G
  hgvsp: ENST00000396596.1:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.186A>G
  hgvsp: ENST00000522629.1:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.186A>G
  hgvsp: ENST00000345714.4:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.516A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.186A>G
  hgvsp: ENST00000521198.2:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.186A>G
  hgvsp: ENST00000518388.1:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.186A>G
  hgvsp: ENST00000519289.1:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/48354
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys62Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

8-67716620-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716620
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716620
    reference: chr 8
allele count: 1
allele frequency: 8.378437253883405e-6
allele num: 119354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.191A>G
  hgvsp: ENSP00000430691.1:p.Gln64Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.191A>G
  hgvsp: ENSP00000429022.1:p.Gln64Arg
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.191A>G
  hgvsp: ENSP00000429606.1:p.Gln64Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.191A>G
  hgvsp: ENSP00000430463.1:p.Gln64Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.-11A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.191A>G
  hgvsp: ENSP00000430256.1:p.Gln64Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.-11A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.191A>G
  hgvsp: ENSP00000379842.1:p.Gln64Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.191A>G
  hgvsp: ENSP00000331816.5:p.Gln64Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-88A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.191A>G
  hgvsp: ENSP00000428972.1:p.Gln64Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.521A>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln64Arg
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-67716648-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716648
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716648
    reference: chr 8
allele count: 1
allele frequency: 8.305509875251242e-6
allele num: 120402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.219T>G
  hgvsp: ENST00000521198.2:c.219T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104205
  ensembl transcript: ENST00000523401
  gene symbol: SGK3
  hgvsc: ENST00000523401.1:n.549T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.219T>G
  hgvsp: ENST00000520976.1:c.219T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.18T>G
  hgvsp: ENST00000521960.1:c.18T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.18T>G
  hgvsp: ENST00000521152.1:c.18T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.219T>G
  hgvsp: ENST00000345714.4:c.219T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.219T>G
  hgvsp: ENST00000396596.1:c.219T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.219T>G
  hgvsp: ENST00000522629.1:c.219T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.219T>G
  hgvsp: ENST00000519289.1:c.219T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-60T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.219T>G
  hgvsp: ENST00000518388.1:c.219T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.219T>G
  hgvsp: ENST00000522398.1:c.219T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro73Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

8-67716683-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716683
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716683
    reference: chr 8
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.52+1G>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.253+1G>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.253+1G>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-26+1G>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.253+1G>C
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.253+1G>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.52+1G>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.253+1G>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.253+1G>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.253+1G>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.253+1G>C
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
hgvs: c.253+1G>C
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

8-67716717-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716717
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716717
    reference: chr 8
allele count: 1
allele frequency: 8.290499088045101e-6
allele num: 120620
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-26+35A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.253+35A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.253+35A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.253+35A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.253+35A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.253+35A>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.253+35A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.253+35A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.253+35A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.52+35A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.52+35A>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44174
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

8-67716725-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716725
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716725
    reference: chr 8
allele count: 34
allele frequency: 2.820500058069119e-4
allele num: 120546
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.253+43A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.253+43A>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.52+43A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.253+43A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.253+43A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.52+43A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.253+43A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.253+43A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-26+43A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.253+43A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.253+43A>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

8-67716731-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716731
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716731
    reference: chr 8
allele count: 1
allele frequency: 8.296138976920141e-6
allele num: 120538
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.253+49A>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.52+49A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.253+49A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.253+49A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-26+49A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.253+49A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.253+49A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.253+49A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.52+49A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.253+49A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.253+49A>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1602
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

8-67716733-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67716733
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67716733
    reference: chr 8
allele count: 2
allele frequency: 1.659695943703114e-5
allele num: 120504
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.253+51G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.253+51G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.253+51G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.253+51G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.253+51G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.253+51G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-26+51G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.253+51G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.52+51G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.52+51G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.253+51G>A
  variant of: http://identifiers.org/hgnc/48354
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ

8-67726040-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726040
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726040
    reference: chr 8
allele count: 10
allele frequency: 8.554466286848363e-5
allele num: 116898
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.254-48T>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.254-48T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.254-48T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.254-48T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8567T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.53-48T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.254-48T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.254-48T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.254-48T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.254-48T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.53-48T>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10771
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15159
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5647
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12824
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3844
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

8-67726043-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726043
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726043
    reference: chr 8
allele count: 1
allele frequency: 8.551393877201984e-6
allele num: 116940
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8564A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.53-45A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.254-45A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.254-45A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.254-45A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.53-45A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.254-45A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.254-45A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.254-45A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.254-45A>T
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.254-45A>T
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6585
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8805
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4627
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

8-67726076-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726076
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726076
    reference: chr 8
allele count: 1
allele frequency: 8.378296859814337e-6
allele num: 119356
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.254-12T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8531T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.53-12T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.254-12T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.254-12T>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.254-12T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.254-12T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.254-12T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.254-12T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.53-12T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.254-12T>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16311
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6317
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS

8-67726079-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726079
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726079
    reference: chr 8
allele count: 1
allele frequency: 8.361343835181191e-6
allele num: 119598
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.254-9C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.53-9C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.254-9C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8528C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.254-9C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.254-9C>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.53-9C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.254-9C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.254-9C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.254-9C>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.254-9C>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1786
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

8-67726084-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726084
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726084
    reference: chr 8
allele count: 31
allele frequency: 2.58341944731491e-4
allele num: 119996
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.254-4C>T
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.254-4C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.254-4C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.53-4C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.254-4C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.254-4C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.254-4C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.254-4C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8523C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.53-4C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.254-4C>T
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28989
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16740
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6202
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: c.254-4C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

8-67726090-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726090
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726090
    reference: chr 8
allele count: 1
allele frequency: 8.305371914554334e-6
allele num: 120404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.256T>G
  hgvsp: ENSP00000430463.1:p.Phe86Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.256T>G
  hgvsp: ENSP00000429606.1:p.Phe86Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.256T>G
  hgvsp: ENSP00000331816.5:p.Phe86Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.256T>G
  hgvsp: ENSP00000379842.1:p.Phe86Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.55T>G
  hgvsp: ENSP00000430475.1:p.Phe19Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.256T>G
  hgvsp: ENSP00000430256.1:p.Phe86Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.55T>G
  hgvsp: ENSP00000429565.1:p.Phe19Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.256T>G
  hgvsp: ENSP00000428972.1:p.Phe86Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.256T>G
  hgvsp: ENSP00000430691.1:p.Phe86Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.256T>G
  hgvsp: ENSP00000429022.1:p.Phe86Val
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8517T>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe86Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-67726095-TAAAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726095
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726091
    reference: chr 8
allele count: 1
allele frequency: 8.295588406085643e-6
allele num: 120546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.265_268delCAAA
  hgvsp: ENSP00000331816.5:p.Gln89AspfsTer5
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.265_268delCAAA
  hgvsp: ENSP00000379842.1:p.Gln89AspfsTer5
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.265_268delCAAA
  hgvsp: ENSP00000429606.1:p.Gln89AspfsTer5
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.64_67delCAAA
  hgvsp: ENSP00000430475.1:p.Gln22AspfsTer5
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.265_268delCAAA
  hgvsp: ENSP00000430463.1:p.Gln89AspfsTer5
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.265_268delCAAA
  hgvsp: ENSP00000428972.1:p.Gln89AspfsTer5
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.265_268delCAAA
  hgvsp: ENSP00000429022.1:p.Gln89AspfsTer5
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.64_67delCAAA
  hgvsp: ENSP00000429565.1:p.Gln22AspfsTer5
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8508_-25-8505delCAAA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.265_268delCAAA
  hgvsp: ENSP00000430691.1:p.Gln89AspfsTer5
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.265_268delCAAA
  hgvsp: ENSP00000430256.1:p.Gln89AspfsTer5
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17015
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln89AspfsTer5
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: TAAAC
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

8-67726097-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726097
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726097
    reference: chr 8
allele count: 1
allele frequency: 8.29132395860971e-6
allele num: 120608
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.62A>G
  hgvsp: ENSP00000429565.1:p.Lys21Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8510A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.263A>G
  hgvsp: ENSP00000430691.1:p.Lys88Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.263A>G
  hgvsp: ENSP00000331816.5:p.Lys88Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.263A>G
  hgvsp: ENSP00000379842.1:p.Lys88Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.62A>G
  hgvsp: ENSP00000430475.1:p.Lys21Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.263A>G
  hgvsp: ENSP00000429022.1:p.Lys88Arg
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.263A>G
  hgvsp: ENSP00000428972.1:p.Lys88Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.263A>G
  hgvsp: ENSP00000430256.1:p.Lys88Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.263A>G
  hgvsp: ENSP00000429606.1:p.Lys88Arg
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.263A>G
  hgvsp: ENSP00000430463.1:p.Lys88Arg
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys88Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

8-67726105-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726105
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726105
    reference: chr 8
allele count: 3
allele frequency: 2.483525944567701e-5
allele num: 120796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.70C>T
  hgvsp: ENSP00000430475.1:p.Arg24Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8502C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.271C>T
  hgvsp: ENSP00000379842.1:p.Arg91Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.271C>T
  hgvsp: ENSP00000430463.1:p.Arg91Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.271C>T
  hgvsp: ENSP00000428972.1:p.Arg91Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.271C>T
  hgvsp: ENSP00000430691.1:p.Arg91Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.70C>T
  hgvsp: ENSP00000429565.1:p.Arg24Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.271C>T
  hgvsp: ENSP00000429606.1:p.Arg91Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.271C>T
  hgvsp: ENSP00000429022.1:p.Arg91Ter
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.271C>T
  hgvsp: ENSP00000430256.1:p.Arg91Ter
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.271C>T
  hgvsp: ENSP00000331816.5:p.Arg91Ter
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17139
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg91Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

8-67726106-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726106
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726106
    reference: chr 8
allele count: 3
allele frequency: 2.482498386376049e-5
allele num: 120846
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.272G>A
  hgvsp: ENSP00000379842.1:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.71G>A
  hgvsp: ENSP00000430475.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8501G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.272G>A
  hgvsp: ENSP00000430256.1:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.272G>A
  hgvsp: ENSP00000430463.1:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.272G>A
  hgvsp: ENSP00000429022.1:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.272G>A
  hgvsp: ENSP00000430691.1:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.272G>A
  hgvsp: ENSP00000331816.5:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.71G>A
  hgvsp: ENSP00000429565.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.272G>A
  hgvsp: ENSP00000429606.1:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.272G>A
  hgvsp: ENSP00000428972.1:p.Arg91Gln
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg91Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/8-67726109-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726109
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726109
    reference: chr 8
allele count: 1
allele frequency: 8.272393368849475e-6
allele num: 120884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.275C>A
  hgvsp: ENSP00000331816.5:p.Ala92Glu
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.275C>A
  hgvsp: ENSP00000428972.1:p.Ala92Glu
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.275C>A
  hgvsp: ENSP00000379842.1:p.Ala92Glu
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.74C>A
  hgvsp: ENSP00000429565.1:p.Ala25Glu
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.275C>A
  hgvsp: ENSP00000429606.1:p.Ala92Glu
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.74C>A
  hgvsp: ENSP00000430475.1:p.Ala25Glu
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.275C>A
  hgvsp: ENSP00000430256.1:p.Ala92Glu
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8498C>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.275C>A
  hgvsp: ENSP00000429022.1:p.Ala92Glu
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.275C>A
  hgvsp: ENSP00000430463.1:p.Ala92Glu
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.275C>A
  hgvsp: ENSP00000430691.1:p.Ala92Glu
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala92Glu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

8-67726120-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726120
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726120
    reference: chr 8
allele count: 15
allele frequency: 1.240387000744232e-4
allele num: 120930
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.85G>A
  hgvsp: ENSP00000429565.1:p.Glu29Lys
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.286G>A
  hgvsp: ENSP00000429022.1:p.Glu96Lys
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.286G>A
  hgvsp: ENSP00000430256.1:p.Glu96Lys
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.286G>A
  hgvsp: ENSP00000428972.1:p.Glu96Lys
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8487G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.286G>A
  hgvsp: ENSP00000429606.1:p.Glu96Lys
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.286G>A
  hgvsp: ENSP00000379842.1:p.Glu96Lys
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.286G>A
  hgvsp: ENSP00000430691.1:p.Glu96Lys
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.286G>A
  hgvsp: ENSP00000430463.1:p.Glu96Lys
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.85G>A
  hgvsp: ENSP00000430475.1:p.Glu29Lys
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.286G>A
  hgvsp: ENSP00000331816.5:p.Glu96Lys
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17233
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu96Lys
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-67726162-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726162
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726162
    reference: chr 8
allele count: 3
allele frequency: 2.489626556016598e-5
allele num: 120500
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.328C>A
  hgvsp: ENSP00000429022.1:p.His110Asn
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.328C>A
  hgvsp: ENSP00000429606.1:p.His110Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.328C>A
  hgvsp: ENSP00000379842.1:p.His110Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.127C>A
  hgvsp: ENSP00000430475.1:p.His43Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.328C>A
  hgvsp: ENSP00000430463.1:p.His110Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.328C>A
  hgvsp: ENSP00000430256.1:p.His110Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8445C>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.328C>A
  hgvsp: ENSP00000331816.5:p.His110Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.127C>A
  hgvsp: ENSP00000429565.1:p.His43Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.328C>A
  hgvsp: ENSP00000428972.1:p.His110Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.328C>A
  hgvsp: ENSP00000430691.1:p.His110Asn
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17309
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6263
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His110Asn
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

8-67726174-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726174
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726174
    reference: chr 8
allele count: 1
allele frequency: 8.351149118118652e-6
allele num: 119744
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8433T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.329+11T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.329+11T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.329+11T>C
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.329+11T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.329+11T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.329+11T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.329+11T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.128+11T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.329+11T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.128+11T>C
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP

8-67726180-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726180
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726180
    reference: chr 8
allele count: 2
allele frequency: 1.676024469957262e-5
allele num: 119330
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.329+17G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.329+17G>A
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.329+17G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.329+17G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.128+17G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.329+17G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.329+17G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.128+17G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.329+17G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8427G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.329+17G>A
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 16692
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

8-67726182-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726182
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726182
    reference: chr 8
allele count: 12
allele frequency: 1.007455168245013e-4
allele num: 119112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.329+19G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.128+19G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.329+19G>A
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.128+19G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.329+19G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.329+19G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8425G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.329+19G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.329+19G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.329+19G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.329+19G>A
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16621
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23347
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6243
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

8-67726184-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726184
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726184
    reference: chr 8
allele count: 1
allele frequency: 8.3948959032908e-6
allele num: 119120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.128+21T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.128+21T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8423T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.329+21T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.329+21T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.329+21T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.329+21T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.329+21T>A
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.329+21T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.329+21T>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.329+21T>A
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

8-67726187-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726187
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726187
    reference: chr 8
allele count: 1
allele frequency: 8.409721638213775e-6
allele num: 118910
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.128+24A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.329+24A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.329+24A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.329+24A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.329+24A>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.329+24A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.329+24A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.329+24A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8420A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.128+24A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.329+24A>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16284
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5912
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

8-67726193-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726193
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726193
    reference: chr 8
allele count: 1
allele frequency: 8.437109783672505e-6
allele num: 118524
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.128+30A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.329+30A>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.329+30A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.329+30A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.128+30A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.329+30A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.329+30A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8414A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.329+30A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.329+30A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.329+30A>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17820
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8019
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5921
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

8-67726210-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67726210
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67726210
    reference: chr 8
allele count: 1
allele frequency: 8.669267446900737e-6
allele num: 115350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.128+47A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.329+47A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.329+47A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.329+47A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.329+47A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.329+47A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.329+47A>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.329+47A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.128+47A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-8397A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.329+47A>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9009
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14530
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6054
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

8-67734561-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734561
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734561
    reference: chr 8
allele count: 3
allele frequency: 2.487397187582913e-5
allele num: 120608
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.330-46G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.330-46G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.330-46G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.330-46G>A
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.129-46G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.129-46G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.330-46G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.330-46G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.330-46G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-46G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.330-46G>A
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3981
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

8-67734568-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734568
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734568
    reference: chr 8
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.330-39T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.129-39T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.330-39T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.129-39T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-39T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.330-39T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.330-39T>C
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.330-39T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.330-39T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.330-39T>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.330-39T>C
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8563
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

8-67734593-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734593
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734593
    reference: chr 8
allele count: 24
allele frequency: 1.983110508833105e-4
allele num: 121022
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.330-14A>T
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.330-14A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.330-14A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-14A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.129-14A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.330-14A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.330-14A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.129-14A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.330-14A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.330-14A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.330-14A>T
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8569
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7513
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3977
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum

8-67734600-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734600
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734600
    reference: chr 8
allele count: 1
allele frequency: 8.256683785524381e-6
allele num: 121114
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.330-7T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.330-7T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.129-7T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.330-7T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.129-7T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.330-7T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-25-7T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.330-7T>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.330-7T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.330-7T>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.330-7T>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.330-7T>G
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-67734608-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734608
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734608
    reference: chr 8
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.331C>A
  hgvsp: ENSP00000429022.1:p.Pro111Thr
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.331C>A
  hgvsp: ENSP00000430463.1:p.Pro111Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.130C>A
  hgvsp: ENSP00000429565.1:p.Pro44Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.331C>A
  hgvsp: ENSP00000429606.1:p.Pro111Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.331C>A
  hgvsp: ENSP00000430691.1:p.Pro111Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.331C>A
  hgvsp: ENSP00000379842.1:p.Pro111Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.130C>A
  hgvsp: ENSP00000430475.1:p.Pro44Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-24C>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.331C>A
  hgvsp: ENSP00000428972.1:p.Pro111Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.331C>A
  hgvsp: ENSP00000331816.5:p.Pro111Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.331C>A
  hgvsp: ENSP00000430256.1:p.Pro111Thr
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8574
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro111Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-67734618-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734618
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734618
    reference: chr 8
allele count: 22
allele frequency: 1.813475773612279e-4
allele num: 121314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-14G>C
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.341G>C
  hgvsp: ENSP00000429022.1:p.Arg114Thr
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.341G>C
  hgvsp: ENSP00000429606.1:p.Arg114Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.341G>C
  hgvsp: ENSP00000379842.1:p.Arg114Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.341G>C
  hgvsp: ENSP00000430256.1:p.Arg114Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.140G>C
  hgvsp: ENSP00000430475.1:p.Arg47Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.140G>C
  hgvsp: ENSP00000429565.1:p.Arg47Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.341G>C
  hgvsp: ENSP00000430691.1:p.Arg114Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.341G>C
  hgvsp: ENSP00000331816.5:p.Arg114Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.341G>C
  hgvsp: ENSP00000428972.1:p.Arg114Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.341G>C
  hgvsp: ENSP00000430463.1:p.Arg114Thr
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 10126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg114Thr
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-67734620-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734620
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734620
    reference: chr 8
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.142G>A
  hgvsp: ENSP00000429565.1:p.Ala48Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.343G>A
  hgvsp: ENSP00000430256.1:p.Ala115Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.343G>A
  hgvsp: ENSP00000430691.1:p.Ala115Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.343G>A
  hgvsp: ENSP00000429606.1:p.Ala115Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.343G>A
  hgvsp: ENSP00000379842.1:p.Ala115Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.343G>A
  hgvsp: ENSP00000428972.1:p.Ala115Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.343G>A
  hgvsp: ENSP00000430463.1:p.Ala115Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.343G>A
  hgvsp: ENSP00000429022.1:p.Ala115Thr
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.343G>A
  hgvsp: ENSP00000331816.5:p.Ala115Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.142G>A
  hgvsp: ENSP00000430475.1:p.Ala48Thr
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-12G>A
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala115Thr
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-67734621-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734621
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734621
    reference: chr 8
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.344C>T
  hgvsp: ENSP00000430691.1:p.Ala115Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.344C>T
  hgvsp: ENSP00000428972.1:p.Ala115Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.344C>T
  hgvsp: ENSP00000429606.1:p.Ala115Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.344C>T
  hgvsp: ENSP00000331816.5:p.Ala115Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.344C>T
  hgvsp: ENSP00000430463.1:p.Ala115Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.344C>T
  hgvsp: ENSP00000429022.1:p.Ala115Val
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.344C>T
  hgvsp: ENSP00000379842.1:p.Ala115Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.143C>T
  hgvsp: ENSP00000429565.1:p.Ala48Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.143C>T
  hgvsp: ENSP00000430475.1:p.Ala48Val
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.344C>T
  hgvsp: ENSP00000430256.1:p.Ala115Val
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala115Val
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-67734634-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734634
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734634
    reference: chr 8
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.156G>A
  hgvsp: ENSP00000429565.1:p.Met52Ile
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.3G>A
  hgvsp: ENSP00000428529.1:p.Met1?
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.156G>A
  hgvsp: ENSP00000430475.1:p.Met52Ile
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.357G>A
  hgvsp: ENSP00000429606.1:p.Met119Ile
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.357G>A
  hgvsp: ENSP00000429022.1:p.Met119Ile
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.357G>A
  hgvsp: ENSP00000331816.5:p.Met119Ile
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.357G>A
  hgvsp: ENSP00000430256.1:p.Met119Ile
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.357G>A
  hgvsp: ENSP00000379842.1:p.Met119Ile
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.357G>A
  hgvsp: ENSP00000430691.1:p.Met119Ile
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.357G>A
  hgvsp: ENSP00000428972.1:p.Met119Ile
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.357G>A
  hgvsp: ENSP00000430463.1:p.Met119Ile
  variant of: http://identifiers.org/hgnc/10812
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

8-67734635-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734635
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734635
    reference: chr 8
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.358G>A
  hgvsp: ENSP00000428972.1:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.358G>A
  hgvsp: ENSP00000430463.1:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.358G>A
  hgvsp: ENSP00000430256.1:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.4G>A
  hgvsp: ENSP00000428529.1:p.Asp2Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.358G>A
  hgvsp: ENSP00000379842.1:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.157G>A
  hgvsp: ENSP00000429565.1:p.Asp53Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.358G>A
  hgvsp: ENSP00000430691.1:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.157G>A
  hgvsp: ENSP00000430475.1:p.Asp53Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.358G>A
  hgvsp: ENSP00000429606.1:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.358G>A
  hgvsp: ENSP00000331816.5:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.358G>A
  hgvsp: ENSP00000429022.1:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/48354
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp120Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

8-67734638-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734638
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734638
    reference: chr 8
allele count: 7
allele frequency: 5.768248265405343e-5
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.361A>G
  hgvsp: ENSP00000379842.1:p.Ser121Gly
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.361A>G
  hgvsp: ENSP00000430463.1:p.Ser121Gly
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.160A>G
  hgvsp: ENSP00000430475.1:p.Ser54Gly
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.160A>G
  hgvsp: ENSP00000429565.1:p.Ser54Gly
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.361A>G
  hgvsp: ENSP00000428972.1:p.Ser121Gly
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.361A>G
  hgvsp: ENSP00000331816.5:p.Ser121Gly
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.361A>G
  hgvsp: ENSP00000429606.1:p.Ser121Gly
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.7A>G
  hgvsp: ENSP00000428529.1:p.Ser3Gly
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.361A>G
  hgvsp: ENSP00000430256.1:p.Ser121Gly
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.361A>G
  hgvsp: ENSP00000430691.1:p.Ser121Gly
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.361A>G
  hgvsp: ENSP00000429022.1:p.Ser121Gly
  variant of: http://identifiers.org/hgnc/48354
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser121Gly
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

8-67734656-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734656
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734656
    reference: chr 8
allele count: 8
allele frequency: 6.592609684543627e-5
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.379G>C
  hgvsp: ENSP00000379842.1:p.Asp127His
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.25G>C
  hgvsp: ENSP00000428529.1:p.Asp9His
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.379G>C
  hgvsp: ENSP00000430691.1:p.Asp127His
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.379G>C
  hgvsp: ENSP00000429022.1:p.Asp127His
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.379G>C
  hgvsp: ENSP00000429606.1:p.Asp127His
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.379G>C
  hgvsp: ENSP00000430256.1:p.Asp127His
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.379G>C
  hgvsp: ENSP00000430463.1:p.Asp127His
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.178G>C
  hgvsp: ENSP00000429565.1:p.Asp60His
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.178G>C
  hgvsp: ENSP00000430475.1:p.Asp60His
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.379G>C
  hgvsp: ENSP00000428972.1:p.Asp127His
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.379G>C
  hgvsp: ENSP00000331816.5:p.Asp127His
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp127His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

8-67734661-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734661
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734661
    reference: chr 8
allele count: 2
allele frequency: 1.648152421135907e-5
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.384A>G
  hgvsp: ENST00000519289.1:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428972
  ensembl transcript: ENST00000518388
  gene symbol: SGK3
  hgvsc: ENST00000518388.1:c.384A>G
  hgvsp: ENST00000518388.1:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.384A>G
  hgvsp: ENST00000522629.1:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.384A>G
  hgvsp: ENST00000345714.4:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.30A>G
  hgvsp: ENST00000519396.1:c.30A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.384A>G
  hgvsp: ENST00000522398.1:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.384A>G
  hgvsp: ENST00000520976.1:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.384A>G
  hgvsp: ENST00000396596.1:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.183A>G
  hgvsp: ENST00000521152.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.183A>G
  hgvsp: ENST00000521960.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.384A>G
  hgvsp: ENST00000521198.2:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro128Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

8-67734701-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734701
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734701
    reference: chr 8
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.417+7A>G
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.417+7A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.417+7A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.216+7A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.417+7A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.417+7A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.417+7A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.417+7A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.216+7A>G
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.63+7A>G
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 8.75e1
  variant carriers: 0
hgvs: c.417+7A>G
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

8-67734702-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734702
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734702
    reference: chr 8
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.216+8G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.216+8G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.417+8G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.63+8G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.417+8G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.417+8G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.417+8G>A
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.417+8G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.417+8G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.417+8G>A
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: c.417+8G>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-67734703-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734703
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734703
    reference: chr 8
allele count: 3
allele frequency: 2.475492623031983e-5
allele num: 121188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.417+9A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.417+9A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.63+9A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.417+9A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.216+9A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.417+9A>T
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.417+9A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.417+9A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.216+9A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.417+9A>T
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24708
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4056
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

8-67734710-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734710
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734710
    reference: chr 8
allele count: 1
allele frequency: 8.261322141995606e-6
allele num: 121046
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.417+16G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.216+16G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.417+16G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.216+16G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.417+16G>A
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.417+16G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.63+16G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.417+16G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.417+16G>A
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.417+16G>A
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13320
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3967
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

8-67734723-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734723
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734724
    reference: chr 8
allele count: 7
allele frequency: 5.796045440996257e-5
allele num: 120772
alternate allele: GA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.417+35dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.417+35dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.417+35dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.216+35dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.417+35dupA
  variant of: http://identifiers.org/hgnc/48354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.417+35dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.417+35dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.417+35dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.63+35dupA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.216+35dupA
  variant of: http://identifiers.org/hgnc/10812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4291
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8489
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8022
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24689
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3956
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

8-67734727-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734727
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734727
    reference: chr 8
allele count: 2
allele frequency: 1.655738790648387e-5
allele num: 120792
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.216+33A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.417+33A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.216+33A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.417+33A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.417+33A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.417+33A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.63+33A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.417+33A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.417+33A>T
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.417+33A>T
  variant of: http://identifiers.org/hgnc/48354
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8456
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5039
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3958
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

8-67734728-AAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67734728
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 67734726
    reference: chr 8
allele count: 1
allele frequency: 8.278556881964336e-6
allele num: 120794
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000379842
  ensembl transcript: ENST00000396596
  gene symbol: SGK3
  hgvsc: ENST00000396596.1:c.417+36_417+37delTA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000428529
  ensembl transcript: ENST00000519396
  gene symbol: SGK3
  hgvsc: ENST00000519396.1:c.63+36_63+37delTA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430691
  ensembl transcript: ENST00000520976
  gene symbol: SGK3
  hgvsc: ENST00000520976.1:c.417+36_417+37delTA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000331816
  ensembl transcript: ENST00000345714
  gene symbol: SGK3
  hgvsc: ENST00000345714.4:c.417+36_417+37delTA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430475
  ensembl transcript: ENST00000521960
  gene symbol: SGK3
  hgvsc: ENST00000521960.1:c.216+36_216+37delTA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430463
  ensembl transcript: ENST00000521198
  gene symbol: SGK3
  hgvsc: ENST00000521198.2:c.417+36_417+37delTA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000430256
  ensembl transcript: ENST00000522398
  gene symbol: SGK3
  hgvsc: ENST00000522398.1:c.417+36_417+37delTA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429606
  ensembl transcript: ENST00000522629
  gene symbol: SGK3
  hgvsc: ENST00000522629.1:c.417+36_417+37delTA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104205
  ensembl protein: ENSP00000429565
  ensembl transcript: ENST00000521152
  gene symbol: SGK3
  hgvsc: ENST00000521152.1:c.216+36_216+37delTA
  variant of: http://identifiers.org/hgnc/10812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000270024
  ensembl protein: ENSP00000429022
  ensembl transcript: ENST00000519289
  gene symbol: C8orf44-SGK3
  hgvsc: ENST00000519289.1:c.417+36_417+37delTA
  variant of: http://identifiers.org/hgnc/48354
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 9757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7680
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3961
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: AAT

GenotypeQuality
all individuals: 309
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1351
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5443
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44943
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1896
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1581
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511532996765319e-5
allele num: 66158
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10076
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.128e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.479e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.958e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.69e0

QD
type: SiteQuality
SIO_000300: 2.8e-1

DP
type: SiteQuality
SIO_000300: 3.70645e6

GenotypeQuality
all individuals: 4944
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1848
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1350
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44942
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10056
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511670093118878e-5
allele num: 66152
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.700397e6

MQRankSum
type: SiteQuality
SIO_000300: -5.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.359e-1

FS
type: SiteQuality
SIO_000300: 3.693e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.208e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 5.58e1

QD
type: SiteQuality
SIO_000300: 3.402e1

GenotypeQuality
all individuals: 878
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3286
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44930
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1182
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9914
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517220452131695e-5
allele num: 65910
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16284
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.83e-1

DP
type: SiteQuality
SIO_000300: 3.684485e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.401e0

VQSLOD
type: SiteQuality
SIO_000300: 4.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.489e1

MQRankSum
type: SiteQuality
SIO_000300: -3.01e-1

GenotypeQuality
all individuals: 1314
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44929
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 3368
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.365167005430331e-4
allele num: 65926
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9914
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.140243153628883e-5
allele num: 16286
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.93e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.08e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 3.167e0

DP
type: SiteQuality
SIO_000300: 3.684161e6

QD
type: SiteQuality
SIO_000300: 1.447e1

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

GenotypeQuality
all individuals: 1455
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3433
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 911
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44927
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 251
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.034993474764029e-5
allele num: 65898
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.142506142506142e-5
allele num: 16280
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.017e0

DP
type: SiteQuality
SIO_000300: 3.683214e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.85e-1

QD
type: SiteQuality
SIO_000300: 1.435e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.983e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.768e0

GenotypeQuality
all individuals: 492
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 842
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1180
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1310
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517542794706811e-5
allele num: 65896
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.313e0

MQRankSum
type: SiteQuality
SIO_000300: 8.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 3.681238e6

QD
type: SiteQuality
SIO_000300: 1.352e1

MQ
type: SiteQuality
SIO_000300: 6.084e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.702e0

GenotypeQuality
all individuals: 1308
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2190
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16224
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9886
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518418415378542e-5
allele num: 65858
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.142e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.28e0

VQSLOD
type: SiteQuality
SIO_000300: -8.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.678393e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.201e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.558e0

GenotypeQuality
all individuals: 1377
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5668
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1327
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3915
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 9478
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 43146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3552
num of homozygotes: 0

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

South Asian
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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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ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQRankSum
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FS
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BaseQRankSum
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MQ
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DP
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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SIO_000300: -1.28e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

QD
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 43260
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6304
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3560
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 9506
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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MQ
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FS
type: SiteQuality
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DP
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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SIO_000300: -5.81e-1

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 13296
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Latino
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allele count: 4
allele frequency: 4.211412929037692e-4
allele num: 9498
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 43192
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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DP
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3594
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 43544
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13352
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9558
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 9.466708740927738e-4
allele num: 6338
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.13e-1

DP
type: SiteQuality
SIO_000300: 9.50169e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-2

FS
type: SiteQuality
SIO_000300: 5.719e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

QD
type: SiteQuality
SIO_000300: 1.84e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13378
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
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allele frequency: 0.0e0
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num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 9.46073793755913e-4
allele num: 6342
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3604
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9572
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 43654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.14e-2

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 5.477e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.0e-3

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 9.65784e5

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 44220
num of homozygotes: 0

South Asian
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allele frequency: 7.437156031533541e-5
allele num: 13446
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Latino
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allele frequency: 0.0e0
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African
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Other
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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
allele num: 3688
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VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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MQ
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 7.320644216691069e-5
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num of homozygotes: 0

European (Finnish)
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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Latino
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ClippingRankSum
type: SiteQuality
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FS
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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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InbreedingCoeff
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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African
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InbreedingCoeff
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1293
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10522
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.019514249613927e-5
allele num: 14246
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50872
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: -3.74e-1

DP
type: SiteQuality
SIO_000300: 1.225811e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 3.319e0

QD
type: SiteQuality
SIO_000300: 8.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.188e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

GenotypeQuality
all individuals: 543
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
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GenotypeQuality
all individuals: 201
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.791325447376403e-5
allele num: 52752
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6088
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10664
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5234
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14554
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 1.549e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.93e0

DP
type: SiteQuality
SIO_000300: 1.261475e6

GenotypeQuality
all individuals: 572
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.149689583812371e-4
allele num: 8698
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7866
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60158
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6252
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.579e1

DP
type: SiteQuality
SIO_000300: 1.376331e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

QD
type: SiteQuality
SIO_000300: 1.511e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.243e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

FS
type: SiteQuality
SIO_000300: 2.393e0

VQSLOD
type: SiteQuality
SIO_000300: -1.726e0

GenotypeDepth
all individuals: 61
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 189
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variant carriers: 0

GenotypeDepth
all individuals: 19
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 41628
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 635
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6723
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64270
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.793527963418924e-5
allele num: 11372
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9402
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.475e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.4e-2

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

DP
type: SiteQuality
SIO_000300: 1.433182e6

GenotypeDepth
all individuals: 179
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 431
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variant carriers: 0

GenotypeDepth
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 1569
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variant carriers: 0

GenotypeQuality
all individuals: 1874
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variant carriers: 0

GenotypeQuality
all individuals: 27
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GenotypeQuality
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GenotypeQuality
all individuals: 6820
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 2359
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 341
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
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variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 42235
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variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.759635599159075e-5
allele num: 11416
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65086
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.43e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.502e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.615e0

DP
type: SiteQuality
SIO_000300: 1.443906e6

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-2

GenotypeDepth
all individuals: 102
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
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variant carriers: 0

GenotypeDepth
all individuals: 129
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1882
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variant carriers: 0

GenotypeQuality
all individuals: 6838
bin: 6.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9540
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531721961829489e-5
allele num: 65286
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.44633e6

VQSLOD
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -7.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 3.7e-2

MQ
type: SiteQuality
SIO_000300: 5.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

QD
type: SiteQuality
SIO_000300: 1.636e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

GenotypeDepth
all individuals: 42
bin: 8.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 16
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GenotypeQuality
all individuals: 50
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 810
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GenotypeQuality
all individuals: 658
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519018106695832e-5
allele num: 65832
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.062e0

QD
type: SiteQuality
SIO_000300: 1.095e1

MQRankSum
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FS
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ReadPosRankSum
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DP
type: SiteQuality
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VQSLOD
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SIO_000300: 2.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.01e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 1918
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GenotypeQuality
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GenotypeQuality
all individuals: 6982
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variant carriers: 0

GenotypeQuality
all individuals: 1597
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

East Asian
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.505978735580254e-5
allele num: 66402
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African
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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VQSLOD
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MQ
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QD
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DP
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SIO_000300: 1.465059e6

ClippingRankSum
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SIO_000300: -4.14e-1

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

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

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

Other
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South Asian
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allele frequency: 0.0e0
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East Asian
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InbreedingCoeff
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ClippingRankSum
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MQ
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VQSLOD
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MQRankSum
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BaseQRankSum
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SIO_000300: -8.42e-1

FS
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ReadPosRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
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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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African
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Other
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.503804625703029e-5
allele num: 66498
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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DP
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QD
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FS
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 8.399999999999999e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 34
allele frequency: 5.114935611987002e-4
allele num: 66472
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Other
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allele num: 908
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Latino
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num of homozygotes: 0

MQRankSum
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SIO_000300: 9.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.75e-1

InbreedingCoeff
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SIO_000300: 2.01e-2

ClippingRankSum
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SIO_000300: -2.66e-1

DP
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SIO_000300: 1.461501e6

BaseQRankSum
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SIO_000300: 4.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.76e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 1
allele frequency: 8.688097306689835e-5
allele num: 11510
num of homozygotes: 0

African
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Other
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European (Non-Finnish)
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ReadPosRankSum
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QD
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MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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DP
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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allele num: 66444
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Latino
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allele num: 11508
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European (Finnish)
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East Asian
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African
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South Asian
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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FS
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QD
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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East Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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South Asian
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FS
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VQSLOD
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DP
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ReadPosRankSum
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QD
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ClippingRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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South Asian
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East Asian
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Latino
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European (Finnish)
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Other
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MQRankSum
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FS
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ReadPosRankSum
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MQ
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QD
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DP
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.25e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 102
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GenotypeQuality
all individuals: 1141
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.347594261774788e-5
allele num: 15754
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 8.69e-1

InbreedingCoeff
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SIO_000300: 2.91e-2

DP
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SIO_000300: 1.698672e6

VQSLOD
type: SiteQuality
SIO_000300: -1.298e0

QD
type: SiteQuality
SIO_000300: 1.927e1

BaseQRankSum
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SIO_000300: 3.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.187e0

GenotypeQuality
all individuals: 241
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515518913676043e-5
allele num: 65984
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15834
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.9e0

FS
type: SiteQuality
SIO_000300: 5.605e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e-1

ClippingRankSum
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SIO_000300: -1.058e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.652e-1

DP
type: SiteQuality
SIO_000300: 1.705137e6

BaseQRankSum
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SIO_000300: 3.15e0

QD
type: SiteQuality
SIO_000300: 9.43e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 31

GenotypeQuality
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GenotypeQuality
all individuals: 451
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 5
allele frequency: 4.348582362149939e-4
allele num: 11498
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16036
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.879953152449736e-4
allele num: 10246
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 21
allele frequency: 3.175947491001482e-4
allele num: 66122
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 4.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -2.9e-2

MQRankSum
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SIO_000300: 3.7e-2

QD
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SIO_000300: 1.169e1

BaseQRankSum
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SIO_000300: -2.711e0

DP
type: SiteQuality
SIO_000300: 1.712931e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.299999999999999e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 454
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GenotypeQuality
all individuals: 1471
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16198
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507977199384745e-5
allele num: 66314
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.718049e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.71e-1

FS
type: SiteQuality
SIO_000300: 6.927e0

VQSLOD
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SIO_000300: -2.836e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

ClippingRankSum
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SIO_000300: 9.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.35e-1

QD
type: SiteQuality
SIO_000300: 2.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.57e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 410
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6439
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66364
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.140997297961189e-5
allele num: 16284
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

FS
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SIO_000300: 0.0e0

QD
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BaseQRankSum
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VQSLOD
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SIO_000300: 2.69e0

MQRankSum
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SIO_000300: 3.15e-1

ReadPosRankSum
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SIO_000300: 1.07e0

DP
type: SiteQuality
SIO_000300: 1.720328e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-1

MQ
type: SiteQuality
SIO_000300: 5.819e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1481
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66394
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.735202492211838e-5
allele num: 10272
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

FS
type: SiteQuality
SIO_000300: 5.969e0

MQRankSum
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DP
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InbreedingCoeff
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SIO_000300: 1.26e-2

ReadPosRankSum
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BaseQRankSum
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SIO_000300: 5.19e0

VQSLOD
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QD
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SIO_000300: 1.564e1

MQ
type: SiteQuality
SIO_000300: 5.587e1

ClippingRankSum
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SIO_000300: -1.209e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1134
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GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.513993379476377e-5
allele num: 66460
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 1.218472036066772e-4
allele num: 16414
num of homozygotes: 0

Other
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DP
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VQSLOD
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ClippingRankSum
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FS
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MQRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 2.4e-2

BaseQRankSum
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SIO_000300: 6.22e-1

QD
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SIO_000300: 1.336e1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.503623733197005e-5
allele num: 66506
num of homozygotes: 0

ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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DP
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

Other
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Latino
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allele frequency: 8.667013347200555e-5
allele num: 11538
num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.953712052900511e-4
allele num: 66540
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.77e-1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16338
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.523113107981787e-5
allele num: 66326
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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QD
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SIO_000300: 1.05e1

MQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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DP
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MQ
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.46e-1

GenotypeQuality
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variant carriers: 1

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65946
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Other
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East Asian
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African
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European (Finnish)
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QD
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MQRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11448
num of homozygotes: 0

South Asian
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allele frequency: 1.2482836100362e-4
allele num: 16022
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East Asian
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African
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European (Non-Finnish)
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Other
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European (Finnish)
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ClippingRankSum
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ReadPosRankSum
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FS
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10102
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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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East Asian
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South Asian
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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FS
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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Latino
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European (Finnish)
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East Asian
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South Asian
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num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.483e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.736e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -8.515e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.655143e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.367e1

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

GenotypeQuality
all individuals: 1861
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5949
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15914
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526857422053929e-5
allele num: 65494
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

QD
type: SiteQuality
SIO_000300: 1.07e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.637041e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.889e0

VQSLOD
type: SiteQuality
SIO_000300: -8.459e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1

GenotypeQuality
all individuals: 30105
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.309944472488642e-5
allele num: 15848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65296
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10040
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.679e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.57e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

QD
type: SiteQuality
SIO_000300: 1.033e1

DP
type: SiteQuality
SIO_000300: 1.59532e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
all individuals: 1040
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variant carriers: 0

GenotypeQuality
all individuals: 3157
bin: 6.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15262
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.576789656259855e-5
allele num: 63420
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.469155e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.49e-1

MQ
type: SiteQuality
SIO_000300: 5.777e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

VQSLOD
type: SiteQuality
SIO_000300: -1.647e0

QD
type: SiteQuality
SIO_000300: 1.919e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.11e-1

GenotypeQuality
all individuals: 238
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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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
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 24745
bin: 9.75e1
variant carriers: 3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10136
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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: 1
allele frequency: 6.157635467980295e-5
allele num: 16240
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007428348019608e-5
allele num: 66502
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.602837e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.751e0

QD
type: SiteQuality
SIO_000300: 1.296e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502945773716484e-5
allele num: 66536
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16262
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.568e1

MQ
type: SiteQuality
SIO_000300: 5.986e1

DP
type: SiteQuality
SIO_000300: 2.607608e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

FS
type: SiteQuality
SIO_000300: 4.453e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.26e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 24

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21654501216545e-4
allele num: 16440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 20
allele frequency: 2.31107002542177e-3
allele num: 8654
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.246e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.028e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.625162e6

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3975
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
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: 904
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.977e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.4222e1

QD
type: SiteQuality
SIO_000300: 1.733e1

ClippingRankSum
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SIO_000300: 5.24e-1

DP
type: SiteQuality
SIO_000300: 2.624545e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

GenotypeDepth
all individuals: 11
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 1910
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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African
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East Asian
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allele num: 8654
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South Asian
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Other
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MQ
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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FS
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DP
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ReadPosRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Non-Finnish)
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Latino
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European (Finnish)
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South Asian
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East Asian
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VQSLOD
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MQ
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QD
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DP
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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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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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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East Asian
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BaseQRankSum
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FS
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DP
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VQSLOD
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MQ
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MQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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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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GenotypeQuality
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Other
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African
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European (Finnish)
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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MQRankSum
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MQ
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DP
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FS
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VQSLOD
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BaseQRankSum
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QD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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East Asian
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Other
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ReadPosRankSum
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DP
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FS
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MQRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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MQ
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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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European (Finnish)
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East Asian
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African
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Latino
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Other
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European (Non-Finnish)
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ClippingRankSum
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DP
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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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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QD
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FS
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InbreedingCoeff
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MQ
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ReadPosRankSum
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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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 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 frequency: 1.199256460994184e-4
allele num: 66708
num of homozygotes: 0

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

South Asian
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FS
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SIO_000300: 1.144e0

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

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

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.998231043684226e-5
allele num: 66706
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Other
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ReadPosRankSum
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BaseQRankSum
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MQ
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FS
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MQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66628
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South Asian
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Latino
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East Asian
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Other
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ReadPosRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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MQ
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ClippingRankSum
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66618
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European (Finnish)
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allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
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
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South Asian
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allele frequency: 0.0e0
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Other
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MQRankSum
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SIO_000300: -6.33e-1

QD
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DP
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VQSLOD
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ClippingRankSum
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FS
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BaseQRankSum
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MQ
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

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

East Asian
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allele frequency: 3.470615455807496e-4
allele num: 8644
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

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

Other
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QD
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SIO_000300: 1.11e1

ReadPosRankSum
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BaseQRankSum
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FS
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MQ
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ClippingRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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European (Finnish)
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Other
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African
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MQRankSum
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VQSLOD
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MQ
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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allele num: 66448
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South Asian
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Latino
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Other
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VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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Latino
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European (Finnish)
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BaseQRankSum
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QD
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DP
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ReadPosRankSum
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MQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5031
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2288
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2135
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11233
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3767
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24683
bin: 9.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504800312998465e-5
allele num: 66454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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