2-233421290-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233421290
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233421290
    reference: chr 2
allele count: 34
allele frequency: 5.656296789219764e-4
allele num: 60110
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.135+50T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000463074
  gene symbol: EIF4E2
  hgvsc: ENST00000463074.1:n.236T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+50T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+50T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.120+50T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.135+50T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.169+50T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+50T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.135+50T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.135+50T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000479834
  gene symbol: EIF4E2
  hgvsc: ENST00000479834.1:n.561+50T>A
  variant of: http://identifiers.org/hgnc/3293
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6863
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13059
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21588
  bin: 7.5e0
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10275
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

2-233421291-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233421291
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233421291
    reference: chr 2
allele count: 33
allele frequency: 5.545845657434794e-4
allele num: 59504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.135+51T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.135+51T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+51T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.169+51T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000479834
  gene symbol: EIF4E2
  hgvsc: ENST00000479834.1:n.561+51T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.120+51T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+51T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000463074
  gene symbol: EIF4E2
  hgvsc: ENST00000463074.1:n.237T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.135+51T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.135+51T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+51T>A
  variant of: http://identifiers.org/hgnc/3293
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21660
  bin: 7.5e0
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13002
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 1.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/2-233421292-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233421292
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233421292
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 55348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+52A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.135+52A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+52A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000479834
  gene symbol: EIF4E2
  hgvsc: ENST00000479834.1:n.561+52A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.120+52A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.135+52A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+52A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.135+52A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000463074
  gene symbol: EIF4E2
  hgvsc: ENST00000463074.1:n.238A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.169+52A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.135+52A>C
  variant of: http://identifiers.org/hgnc/3293
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 12889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6893
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6081
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

2-233422546-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422546
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422546
    reference: chr 2
allele count: 1
allele frequency: 8.504269143109841e-6
allele num: 117588
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1306G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.121-48G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1306G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.136-48G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.136-48G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.170-48G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1306G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.136-48G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.136-48G>C
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1510
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

2-233422549-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422549
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422549
    reference: chr 2
allele count: 1
allele frequency: 8.511217785040683e-6
allele num: 117492
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.136-45C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1309C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.136-45C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.136-45C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.170-45C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1309C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1309C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.136-45C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.121-45C>G
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

2-233422551-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422551
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422551
    reference: chr 2
allele count: 7
allele frequency: 5.954710175749017e-5
allele num: 117554
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.136-43C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1311C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.121-43C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.136-43C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.136-43C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.136-43C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.170-43C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1311C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1311C>T
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6046
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2071
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1107
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

2-233422552-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422552
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422552
    reference: chr 2
allele count: 1
allele frequency: 8.497620666213461e-6
allele num: 117680
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.136-42G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1312G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.136-42G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1312G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1312G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.136-42G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.136-42G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.121-42G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.170-42G>A
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6391
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2496
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1658
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP

2-233422564-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422564
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422564
    reference: chr 2
allele count: 1
allele frequency: 8.474719910506958e-6
allele num: 117998
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.136-30C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.170-30C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1324C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1324C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.136-30C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.121-30C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.136-30C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.136-30C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1324C>T
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6391
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1643
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2497
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2848
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-233422571-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422571
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422571
    reference: chr 2
allele count: 1
allele frequency: 8.450513791238508e-6
allele num: 118336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1331A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1331A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.170-23A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.121-23A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.136-23A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.136-23A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.136-23A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.136-23A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1331A>G
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6391
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6048
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3694
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

2-233422575-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422575
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422575
    reference: chr 2
allele count: 2
allele frequency: 1.688248104941502e-5
allele num: 118466
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.136-19C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1335C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.170-19C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1335C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.136-19C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.136-19C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.136-19C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1335C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.121-19C>T
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/2-233422576-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422576
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422576
    reference: chr 2
allele count: 1
allele frequency: 8.43113449345744e-6
allele num: 118608
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.121-18A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1336A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.136-18A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1336A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.170-18A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.136-18A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.136-18A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.136-18A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1336A>C
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6391
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7313
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4010
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1515
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/2-233422585-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422585
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422585
    reference: chr 2
allele count: 12
allele frequency: 1.006846556584777e-4
allele num: 119184
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.136-9A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.121-9A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.170-9A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1345A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1345A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.136-9A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1345A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.136-9A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.136-9A>C
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6391
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4845
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1517
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

2-233422602-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422602
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422602
    reference: chr 2
allele count: 1
allele frequency: 8.301097405076952e-6
allele num: 120466
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1362C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.144C>T
  hgvsp: ENST00000409514.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.144C>T
  hgvsp: ENST00000409495.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.144C>T
  hgvsp: ENST00000409098.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.129C>T
  hgvsp: ENST00000454501.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.144C>T
  hgvsp: ENST00000258416.3:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1362C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1362C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.178C>T
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6055
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7086
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2508
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2106
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val48Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum

2-233422610-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422610
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422610
    reference: chr 2
allele count: 1
allele frequency: 8.279105194310599e-6
allele num: 120786
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.152C>G
  hgvsp: ENSP00000258416.3:p.Pro51Arg
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.152C>G
  hgvsp: ENSP00000387336.1:p.Pro51Arg
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1370C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.137C>G
  hgvsp: ENSP00000390904.1:p.Pro46Arg
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1370C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.152C>G
  hgvsp: ENSP00000386996.1:p.Pro51Arg
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.152C>G
  hgvsp: ENSP00000386876.1:p.Pro51Arg
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1370C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.186C>G
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6391
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7086
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41298
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1955
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro51Arg
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

2-233422610-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422610
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422610
    reference: chr 2
allele count: 30
allele frequency: 2.48373155829318e-4
allele num: 120786
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.152C>T
  hgvsp: ENSP00000387336.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.152C>T
  hgvsp: ENSP00000386876.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.152C>T
  hgvsp: ENSP00000386996.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.186C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1370C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1370C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.137C>T
  hgvsp: ENSP00000390904.1:p.Pro46Leu
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.152C>T
  hgvsp: ENSP00000258416.3:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1370C>T
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7086
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6391
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 9.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1955
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1516
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro51Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

2-233422611-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422611
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422611
    reference: chr 2
allele count: 1
allele frequency: 8.274309922552459e-6
allele num: 120856
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.138G>A
  hgvsp: ENST00000454501.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.153G>A
  hgvsp: ENST00000409514.1:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1371G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.153G>A
  hgvsp: ENST00000258416.3:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1371G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.153G>A
  hgvsp: ENST00000409098.1:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.153G>A
  hgvsp: ENST00000409495.1:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1371G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.187G>A
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5067
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2118
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6703
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro51Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

2-233422612-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422612
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422612
    reference: chr 2
allele count: 3
allele frequency: 2.481635894381576e-5
allele num: 120888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.154G>A
  hgvsp: ENSP00000386876.1:p.Ala52Thr
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.188G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.154G>A
  hgvsp: ENSP00000258416.3:p.Ala52Thr
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.154G>A
  hgvsp: ENSP00000386996.1:p.Ala52Thr
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.139G>A
  hgvsp: ENSP00000390904.1:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1372G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.154G>A
  hgvsp: ENSP00000387336.1:p.Ala52Thr
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1372G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1372G>A
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5067
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala52Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

2-233422617-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422617
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422617
    reference: chr 2
allele count: 1
allele frequency: 8.262277744728666e-6
allele num: 121032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.144G>A
  hgvsp: ENST00000454501.1:c.144G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.159G>A
  hgvsp: ENST00000409098.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1377G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.159G>A
  hgvsp: ENST00000409495.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1377G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1377G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.159G>A
  hgvsp: ENST00000409514.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.159G>A
  hgvsp: ENST00000258416.3:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.193G>A
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1983
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41290
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu53Glu
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD

2-233422621-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422621
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422621
    reference: chr 2
allele count: 3
allele frequency: 2.477250582153887e-5
allele num: 121102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1381C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.163C>T
  hgvsp: ENSP00000258416.3:p.Pro55Ser
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1381C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.163C>T
  hgvsp: ENSP00000386996.1:p.Pro55Ser
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.148C>T
  hgvsp: ENSP00000390904.1:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.163C>T
  hgvsp: ENSP00000386876.1:p.Pro55Ser
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1381C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.197C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.163C>T
  hgvsp: ENSP00000387336.1:p.Pro55Ser
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7092
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41291
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro55Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

2-233422634-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422634
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422634
    reference: chr 2
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.176A>G
  hgvsp: ENSP00000258416.3:p.Asn59Ser
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.176A>G
  hgvsp: ENSP00000386996.1:p.Asn59Ser
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1394A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.176A>G
  hgvsp: ENSP00000386876.1:p.Asn59Ser
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1394A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1394A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.176A>G
  hgvsp: ENSP00000387336.1:p.Asn59Ser
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.161A>G
  hgvsp: ENSP00000390904.1:p.Asn54Ser
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.210A>G
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7091
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2007
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41288
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn59Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

2-233422636-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422636
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422636
    reference: chr 2
allele count: 13
allele frequency: 1.072023485560668e-4
allele num: 121266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1396T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.178T>C
  hgvsp: ENSP00000386996.1:p.Tyr60His
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.178T>C
  hgvsp: ENSP00000386876.1:p.Tyr60His
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1396T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.212T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.178T>C
  hgvsp: ENSP00000387336.1:p.Tyr60His
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.163T>C
  hgvsp: ENSP00000390904.1:p.Tyr55His
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1396T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.178T>C
  hgvsp: ENSP00000258416.3:p.Tyr60His
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7091
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7089
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr60His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

2-233422639-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422639
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422639
    reference: chr 2
allele count: 2
allele frequency: 1.649103712132456e-5
allele num: 121278
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.181A>G
  hgvsp: ENSP00000258416.3:p.Thr61Ala
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.215A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.181A>G
  hgvsp: ENSP00000386996.1:p.Thr61Ala
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1399A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.166A>G
  hgvsp: ENSP00000390904.1:p.Thr56Ala
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.181A>G
  hgvsp: ENSP00000386876.1:p.Thr61Ala
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1399A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.181A>G
  hgvsp: ENSP00000387336.1:p.Thr61Ala
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1399A>G
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7091
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7093
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2002
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr61Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

2-233422653-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422653
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422653
    reference: chr 2
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1413C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.195C>T
  hgvsp: ENST00000409098.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.180C>T
  hgvsp: ENST00000454501.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.229C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.195C>T
  hgvsp: ENST00000409514.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1413C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.195C>T
  hgvsp: ENST00000258416.3:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.195C>T
  hgvsp: ENST00000409495.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1413C>T
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7091
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6068
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2010
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2509
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser65Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

2-233422662-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422662
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422662
    reference: chr 2
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.238C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1422C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1422C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1422C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.204C>G
  hgvsp: ENST00000409495.1:c.204C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.189C>G
  hgvsp: ENST00000454501.1:c.189C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.204C>G
  hgvsp: ENST00000258416.3:c.204C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.204C>G
  hgvsp: ENST00000409514.1:c.204C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.204C>G
  hgvsp: ENST00000409098.1:c.204C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2507
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr68Thr
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

2-233422665-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422665
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422665
    reference: chr 2
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.207C>T
  hgvsp: ENST00000409514.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.207C>T
  hgvsp: ENST00000409495.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.207C>T
  hgvsp: ENST00000258416.3:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.207C>T
  hgvsp: ENST00000409098.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1425C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1425C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.241C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.192C>T
  hgvsp: ENST00000454501.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1425C>T
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro69Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

2-233422666-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422666
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422666
    reference: chr 2
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.208G>A
  hgvsp: ENSP00000387336.1:p.Gly70Ser
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.208G>A
  hgvsp: ENSP00000258416.3:p.Gly70Ser
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1426G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.208G>A
  hgvsp: ENSP00000386876.1:p.Gly70Ser
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.208G>A
  hgvsp: ENSP00000386996.1:p.Gly70Ser
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1426G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.193G>A
  hgvsp: ENSP00000390904.1:p.Gly65Ser
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1426G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.242G>A
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly70Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

2-233422671-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422671
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422671
    reference: chr 2
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.213T>C
  hgvsp: ENST00000258416.3:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1431T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.213T>C
  hgvsp: ENST00000409514.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1431T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1431T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.247T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.198T>C
  hgvsp: ENST00000454501.1:c.198T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.213T>C
  hgvsp: ENST00000409495.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.213T>C
  hgvsp: ENST00000409098.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2131
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg71Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

2-233422674-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422674
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422674
    reference: chr 2
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1434C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.216C>T
  hgvsp: ENST00000409098.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1434C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.201C>T
  hgvsp: ENST00000454501.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.216C>T
  hgvsp: ENST00000258416.3:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.216C>T
  hgvsp: ENST00000409514.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.250C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1434C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.216C>T
  hgvsp: ENST00000409495.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2130
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2011
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro72Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum

2-233422677-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422677
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422677
    reference: chr 2
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.253G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.219G>A
  hgvsp: ENST00000258416.3:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1437G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.219G>A
  hgvsp: ENST00000409495.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.219G>A
  hgvsp: ENST00000409098.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1437G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.204G>A
  hgvsp: ENST00000454501.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.219G>A
  hgvsp: ENST00000409514.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1437G>A
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5073
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2508
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr73Thr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

2-233422679-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422679
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422679
    reference: chr 2
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1439G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.206G>A
  hgvsp: ENSP00000390904.1:p.Ser69Asn
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.221G>A
  hgvsp: ENSP00000387336.1:p.Ser74Asn
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.221G>A
  hgvsp: ENSP00000386876.1:p.Ser74Asn
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1439G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1439G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.221G>A
  hgvsp: ENSP00000386996.1:p.Ser74Asn
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.255G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.221G>A
  hgvsp: ENSP00000258416.3:p.Ser74Asn
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2128
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2509
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser74Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/2-233422683-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422683
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422683
    reference: chr 2
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.225A>C
  hgvsp: ENST00000258416.3:c.225A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.225A>C
  hgvsp: ENST00000409514.1:c.225A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.225A>C
  hgvsp: ENST00000409098.1:c.225A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.210A>C
  hgvsp: ENST00000454501.1:c.210A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1443A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1443A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1443A>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.225A>C
  hgvsp: ENST00000409495.1:c.225A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.259A>C
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser75Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

2-233422692-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422692
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422692
    reference: chr 2
allele count: 2
allele frequency: 1.649593375233005e-5
allele num: 121242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.234T>C
  hgvsp: ENST00000409495.1:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.219T>C
  hgvsp: ENST00000454501.1:c.219T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.234T>C
  hgvsp: ENST00000409514.1:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.234T>C
  hgvsp: ENST00000409098.1:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1452T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.234T>C
  hgvsp: ENST00000258416.3:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.268T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1452T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1452T>C
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr78Tyr
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

2-233422695-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422695
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422695
    reference: chr 2
allele count: 8
allele frequency: 6.599679915524098e-5
allele num: 121218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1455A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.271A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.237A>G
  hgvsp: ENST00000409514.1:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.237A>G
  hgvsp: ENST00000258416.3:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.222A>G
  hgvsp: ENST00000454501.1:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1455A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1455A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.237A>G
  hgvsp: ENST00000409098.1:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.237A>G
  hgvsp: ENST00000409495.1:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41282
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 2130
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu79Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD

2-233422710-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422710
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422710
    reference: chr 2
allele count: 4
allele frequency: 3.306058351929912e-5
allele num: 120990
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.237G>A
  hgvsp: ENST00000454501.1:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.286G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1470G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1470G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.252G>A
  hgvsp: ENST00000409098.1:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.252G>A
  hgvsp: ENST00000258416.3:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.252G>A
  hgvsp: ENST00000409514.1:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.252G>A
  hgvsp: ENST00000409495.1:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1470G>A
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gln84Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/2-233422718-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422718
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422718
    reference: chr 2
allele count: 1
allele frequency: 8.283082632032337e-6
allele num: 120728
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1478C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.294C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.260C>A
  hgvsp: ENSP00000386996.1:p.Thr87Asn
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.260C>A
  hgvsp: ENSP00000387336.1:p.Thr87Asn
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1478C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.245C>A
  hgvsp: ENSP00000390904.1:p.Thr82Asn
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.260C>A
  hgvsp: ENSP00000258416.3:p.Thr87Asn
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1478C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.260C>A
  hgvsp: ENSP00000386876.1:p.Thr87Asn
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5073
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6055
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1154
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr87Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

2-233422728-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422728
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422728
    reference: chr 2
allele count: 4
allele frequency: 3.325131342688036e-5
allele num: 120296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.270T>A
  hgvsp: ENST00000409495.1:c.270T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.304T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1488T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.270T>A
  hgvsp: ENST00000409514.1:c.270T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.255T>A
  hgvsp: ENST00000454501.1:c.255T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.270T>A
  hgvsp: ENST00000258416.3:c.270T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.270T>A
  hgvsp: ENST00000409098.1:c.270T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1488T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1488T>A
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2110
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5157
  bin: 6.25e1
  variant carriers: 0
hgvs: c.270T>A
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

2-233422731-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422731
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422731
    reference: chr 2
allele count: 8
allele frequency: 6.652917304237908e-5
allele num: 120248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.270+3G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.270+3G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1491G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.307G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.270+3G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.255+3G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.270+3G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1491G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1491G>A
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7086
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41271
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1846
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 2.25e1
  variant carriers: 0
hgvs: c.270+3G>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/2-233422736-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422736
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422736
    reference: chr 2
allele count: 2
allele frequency: 1.665168015452759e-5
allele num: 120108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1496C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.270+8C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1496C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.270+8C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.255+8C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1496C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.312C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.270+8C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.270+8C>A
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6052
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1515
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41267
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: c.270+8C>A
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

2-233422745-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422745
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422745
    reference: chr 2
allele count: 1
allele frequency: 8.342092530490349e-6
allele num: 119874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.270+17T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.321T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1505T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.255+17T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.270+17T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1505T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.270+17T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.270+17T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1505T>A
  variant of: http://identifiers.org/hgnc/3293
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41266
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4249
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1688
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD

2-233422746-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422746
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422746
    reference: chr 2
allele count: 1
allele frequency: 8.34306691139663e-6
allele num: 119860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.270+18T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.322T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.270+18T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1506T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.255+18T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.270+18T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1506T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.270+18T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1506T>A
  variant of: http://identifiers.org/hgnc/3293
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1514
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2852
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD

2-233422755-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422755
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422755
    reference: chr 2
allele count: 1
allele frequency: 8.353241893178742e-6
allele num: 119714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.270+27G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.331G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.270+27G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.255+27G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.270+27G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1515G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.270+27G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1515G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1515G>A
  variant of: http://identifiers.org/hgnc/3293
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2490
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

2-233422758-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422758
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422758
    reference: chr 2
allele count: 1
allele frequency: 8.369741709770836e-6
allele num: 119478
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.270+30C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1518C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.270+30C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1518C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.334C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.270+30C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.255+30C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.270+30C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1518C>T
  variant of: http://identifiers.org/hgnc/3293
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7082
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6052
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2003
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

2-233422769-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422769
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422769
    reference: chr 2
allele count: 3
allele frequency: 2.519907267412559e-5
allele num: 119052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.255+41C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.270+41C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1529C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.270+41C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1529C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.270+41C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.270+41C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.345C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1529C>T
  variant of: http://identifiers.org/hgnc/3293
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1992
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2083
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2845
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

2-233422770-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422770
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422770
    reference: chr 2
allele count: 5
allele frequency: 4.206204993606568e-5
allele num: 118872
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.255+42G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1530G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1530G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.270+42G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.270+42G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.346G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1530G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.270+42G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.270+42G>A
  variant of: http://identifiers.org/hgnc/3293
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

2-233422770-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422770
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422770
    reference: chr 2
allele count: 1
allele frequency: 8.412409987213136e-6
allele num: 118872
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.270+42G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1530G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.255+42G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.346G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1530G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.270+42G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1530G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.270+42G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.270+42G>T
  variant of: http://identifiers.org/hgnc/3293
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2223
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1662
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2485
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-233422771-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422771
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422771
    reference: chr 2
allele count: 26
allele frequency: 2.185755598897034e-4
allele num: 118952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1531T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1531T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.270+43T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.347T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.270+43T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.270+43T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.270+43T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.255+43T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1531T>C
  variant of: http://identifiers.org/hgnc/3293
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7081
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5073
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4647
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3251
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6051
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2082
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2485
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

2-233422774-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422774
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422774
    reference: chr 2
allele count: 6
allele frequency: 5.04999495000505e-5
allele num: 118812
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1534A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1534A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.270+46A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.255+46A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.270+46A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1534A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.350A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.270+46A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.270+46A>G
  variant of: http://identifiers.org/hgnc/3293
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6402
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5067
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6048
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7315
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1842
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2149
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

2-233422780-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233422780
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233422780
    reference: chr 2
allele count: 1
allele frequency: 8.463530646444471e-6
allele num: 118154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.270+52G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.135+1540G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.255+52G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.270+52G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.270+52G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.135+1540G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.270+52G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135930
  ensembl transcript: ENST00000498242
  gene symbol: EIF4E2
  hgvsc: ENST00000498242.1:n.356G>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.135+1540G>A
  variant of: http://identifiers.org/hgnc/3293
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7082
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1520
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1507
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1063
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

2-233428907-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428907
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428907
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 24584
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.136-50A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.136-50A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.256-50A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.271-50A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.271-50A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.271-50A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.271-50A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.136-50A>G
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28612
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17173
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4487
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7471
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19448
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

2-233428917-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428917
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428917
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 24926
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.271-40A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.136-40A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.271-40A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.136-40A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.256-40A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.271-40A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.136-40A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.271-40A>G
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18846
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 946
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6068
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3112
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21763
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12392
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

2-233428918-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428918
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428918
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 24986
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.271-39A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.256-39A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.136-39A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.271-39A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.271-39A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.136-39A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.136-39A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.271-39A>G
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26800
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3661
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3474
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5755
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

2-233428923-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428923
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428923
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 25460
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.271-34A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.136-34A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.136-34A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.271-34A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.271-34A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.256-34A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.136-34A>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.271-34A>G
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 21554
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24696
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4497
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3117
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16780
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/2-233428924-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428924
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428924
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 25534
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.271-33C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.271-33C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.256-33C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.271-33C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.136-33C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.136-33C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.136-33C>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.271-33C>A
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22059
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24184
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4241
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17435
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20787
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1003
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

2-233428926-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428926
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428926
    reference: chr 2
allele count: 2
allele frequency: 7.743534148985597e-5
allele num: 25828
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.136-31T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.136-31T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.271-31T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.271-31T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.271-31T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.256-31T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.136-31T>A
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.271-31T>A
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22997
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3847
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4099
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18353
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3123
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

2-233428927-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428927
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428927
    reference: chr 2
allele count: 11246
allele frequency: 3.435571576953626e-1
allele num: 32734
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.256-30G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.271-30G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.271-30G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.136-30G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.271-30G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.271-30G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.136-30G>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.136-30G>C
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16548
  bin: 2.5e0
  variant carriers: 1712
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 1.75e1
  variant carriers: 1004
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.25e1
  variant carriers: 561
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 2.75e1
  variant carriers: 642
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 9.75e1
  variant carriers: 839
genotype depth: GenotypeDepth
  all individuals: 5359
  bin: 1.25e1
  variant carriers: 3855
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 24418
  bin: 7.5e0
  variant carriers: 9218
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 233
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 195
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 3.75e1
  variant carriers: 435
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 2.25e1
  variant carriers: 631
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 268
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 173
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 176
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.75e1
  variant carriers: 116
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 7.75e1
  variant carriers: 255
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 5.25e1
  variant carriers: 216
genotype quality: GenotypeQuality
  all individuals: 1499
  bin: 2.75e1
  variant carriers: 952
genotype quality: GenotypeQuality
  all individuals: 11774
  bin: 7.5e0
  variant carriers: 589
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 8.25e1
  variant carriers: 177
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 4.75e1
  variant carriers: 139
genotype quality: GenotypeQuality
  all individuals: 2487
  bin: 1.75e1
  variant carriers: 1296
genotype quality: GenotypeQuality
  all individuals: 11951
  bin: 9.75e1
  variant carriers: 10830
num of homozygotes: 1710
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

2-233428927-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428927
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428927
    reference: chr 2
allele count: 3
allele frequency: 9.164782794647767e-5
allele num: 32734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.271-30G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.256-30G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.271-30G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.271-30G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.271-30G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.136-30G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.136-30G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.136-30G>T
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24418
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16548
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5359
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1499
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2487
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11220
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11774
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6113
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

2-233428927-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428927
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428926
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 32734
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.271-24delT
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.256-24delT
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.271-24delT
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.271-24delT
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.136-24delT
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.271-24delT
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.136-24delT
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.136-24delT
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 24418
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11774
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2563
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1499
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2487
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6113
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: GT
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

2-233428938-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428938
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428938
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 34028
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.136-19T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.256-19T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.271-19T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.271-19T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.271-19T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.136-19T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.136-19T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.271-19T>C
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29279
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13719
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4855
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5916
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1766
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12160
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-233428939-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428939
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428939
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 34096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.271-18G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.136-18G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.271-18G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.271-18G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.256-18G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.136-18G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.271-18G>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.136-18G>T
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29660
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11785
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2033
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2444
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

2-233428949-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428949
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428949
    reference: chr 2
allele count: 1
allele frequency: 2.693820376057325e-5
allele num: 37122
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.271-8C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.136-8C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.271-8C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.271-8C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.136-8C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.256-8C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.136-8C>G
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.271-8C>G
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9003
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8463
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1703
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31019
  bin: 2.25e1
  variant carriers: 0
hgvs: c.271-8C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

2-233428949-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428949
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428949
    reference: chr 2
allele count: 78
allele frequency: 2.101179893324713e-3
allele num: 37122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.136-8C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.271-8C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.271-8C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.271-8C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.136-8C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.271-8C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.256-8C>T
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.136-8C>T
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9003
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32624
  bin: 7.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 5962
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
hgvs: c.271-8C>T
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

2-233428952-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428952
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428952
    reference: chr 2
allele count: 1
allele frequency: 2.61437908496732e-5
allele num: 38250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.271-5T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.136-5T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.271-5T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.256-5T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.136-5T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.271-5T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.136-5T>C
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.271-5T>C
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8078
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7655
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1189
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1559
  bin: 2.75e1
  variant carriers: 0
hgvs: c.271-5T>C
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

2-233428981-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428981
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428981
    reference: chr 2
allele count: 1
allele frequency: 2.082899395959175e-5
allele num: 48010
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.280A>G
  hgvsp: ENSP00000390904.1:p.Ser94Gly
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.160A>G
  hgvsp: ENSP00000386424.1:p.Ser54Gly
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.295A>G
  hgvsp: ENSP00000258416.3:p.Ser99Gly
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.295A>G
  hgvsp: ENSP00000387336.1:p.Ser99Gly
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.160A>G
  hgvsp: ENSP00000386983.1:p.Ser54Gly
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.160A>G
  hgvsp: ENSP00000387328.3:p.Ser54Gly
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.295A>G
  hgvsp: ENSP00000386876.1:p.Ser99Gly
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.295A>G
  hgvsp: ENSP00000386996.1:p.Ser99Gly
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2291
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser99Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

2-233428987-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428987
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428987
    reference: chr 2
allele count: 1
allele frequency: 2.033429582333564e-5
allele num: 49178
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.286A>G
  hgvsp: ENSP00000390904.1:p.Met96Val
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.166A>G
  hgvsp: ENSP00000386424.1:p.Met56Val
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.166A>G
  hgvsp: ENSP00000387328.3:p.Met56Val
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.166A>G
  hgvsp: ENSP00000386983.1:p.Met56Val
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.301A>G
  hgvsp: ENSP00000387336.1:p.Met101Val
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.301A>G
  hgvsp: ENSP00000386996.1:p.Met101Val
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.301A>G
  hgvsp: ENSP00000386876.1:p.Met101Val
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.301A>G
  hgvsp: ENSP00000258416.3:p.Met101Val
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32628
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3918
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Met101Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-233428993-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428993
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428993
    reference: chr 2
allele count: 1
allele frequency: 2.026670990231446e-5
allele num: 49342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.307C>T
  hgvsp: ENSP00000386876.1:p.Arg103Cys
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.172C>T
  hgvsp: ENSP00000386424.1:p.Arg58Cys
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.307C>T
  hgvsp: ENSP00000386996.1:p.Arg103Cys
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.292C>T
  hgvsp: ENSP00000390904.1:p.Arg98Cys
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.172C>T
  hgvsp: ENSP00000386983.1:p.Arg58Cys
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.307C>T
  hgvsp: ENSP00000387336.1:p.Arg103Cys
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.307C>T
  hgvsp: ENSP00000258416.3:p.Arg103Cys
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.172C>T
  hgvsp: ENSP00000387328.3:p.Arg58Cys
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31691
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12592
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3987
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg103Cys
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

2-233428995-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428995
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428995
    reference: chr 2
allele count: 1
allele frequency: 2.014666774115561e-5
allele num: 49636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.309T>C
  hgvsp: ENST00000409514.1:c.309T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.309T>C
  hgvsp: ENST00000409098.1:c.309T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.174T>C
  hgvsp: ENST00000409167.3:c.174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.174T>C
  hgvsp: ENST00000409394.1:c.174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.174T>C
  hgvsp: ENST00000409322.1:c.174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.294T>C
  hgvsp: ENST00000454501.1:c.294T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.309T>C
  hgvsp: ENST00000409495.1:c.309T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.309T>C
  hgvsp: ENST00000258416.3:c.309T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4028
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg103Arg
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP

2-233428998-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233428998
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233428998
    reference: chr 2
allele count: 1
allele frequency: 2.016616923449222e-5
allele num: 49588
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.177T>C
  hgvsp: ENST00000409322.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.177T>C
  hgvsp: ENST00000409167.3:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.312T>C
  hgvsp: ENST00000409098.1:c.312T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.177T>C
  hgvsp: ENST00000409394.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.312T>C
  hgvsp: ENST00000409495.1:c.312T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.312T>C
  hgvsp: ENST00000258416.3:c.312T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.297T>C
  hgvsp: ENST00000454501.1:c.297T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.312T>C
  hgvsp: ENST00000409514.1:c.312T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4057
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4920
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31467
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro104Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/2-233429005-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233429005
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233429005
    reference: chr 2
allele count: 2
allele frequency: 4.096178265678122e-5
allele num: 48826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.184C>A
  hgvsp: ENSP00000386424.1:p.Leu62Met
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.184C>A
  hgvsp: ENSP00000386983.1:p.Leu62Met
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.184C>A
  hgvsp: ENSP00000387328.3:p.Leu62Met
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.319C>A
  hgvsp: ENSP00000386996.1:p.Leu107Met
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.304C>A
  hgvsp: ENSP00000390904.1:p.Leu102Met
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.319C>A
  hgvsp: ENSP00000387336.1:p.Leu107Met
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.319C>A
  hgvsp: ENSP00000386876.1:p.Leu107Met
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.319C>A
  hgvsp: ENSP00000258416.3:p.Leu107Met
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5747
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1728
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu107Met
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-233429005-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233429005
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233429005
    reference: chr 2
allele count: 1
allele frequency: 2.048089132839061e-5
allele num: 48826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.184C>T
  hgvsp: ENST00000409322.1:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.319C>T
  hgvsp: ENST00000409098.1:c.319C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.319C>T
  hgvsp: ENST00000409514.1:c.319C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.304C>T
  hgvsp: ENST00000454501.1:c.304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.184C>T
  hgvsp: ENST00000409167.3:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.184C>T
  hgvsp: ENST00000409394.1:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.319C>T
  hgvsp: ENST00000409495.1:c.319C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.319C>T
  hgvsp: ENST00000258416.3:c.319C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5747
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu107Leu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

2-233429040-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 233429040
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 233429040
    reference: chr 2
allele count: 4
allele frequency: 9.543350670420384e-5
allele num: 41914
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000390904
  ensembl transcript: ENST00000454501
  gene symbol: EIF4E2
  hgvsc: ENST00000454501.1:c.339A>T
  hgvsp: ENSP00000390904.1:p.Glu113Asp
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386876
  ensembl transcript: ENST00000409495
  gene symbol: EIF4E2
  hgvsc: ENST00000409495.1:c.354A>T
  hgvsp: ENSP00000386876.1:p.Glu118Asp
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387336
  ensembl transcript: ENST00000409514
  gene symbol: EIF4E2
  hgvsc: ENST00000409514.1:c.354A>T
  hgvsp: ENSP00000387336.1:p.Glu118Asp
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386996
  ensembl transcript: ENST00000409098
  gene symbol: EIF4E2
  hgvsc: ENST00000409098.1:c.354A>T
  hgvsp: ENSP00000386996.1:p.Glu118Asp
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386983
  ensembl transcript: ENST00000409394
  gene symbol: EIF4E2
  hgvsc: ENST00000409394.1:c.219A>T
  hgvsp: ENSP00000386983.1:p.Glu73Asp
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000258416
  ensembl transcript: ENST00000258416
  gene symbol: EIF4E2
  hgvsc: ENST00000258416.3:c.354A>T
  hgvsp: ENSP00000258416.3:p.Glu118Asp
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000386424
  ensembl transcript: ENST00000409322
  gene symbol: EIF4E2
  hgvsc: ENST00000409322.1:c.219A>T
  hgvsp: ENSP00000386424.1:p.Glu73Asp
  variant of: http://identifiers.org/hgnc/3293
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135930
  ensembl protein: ENSP00000387328
  ensembl transcript: ENST00000409167
  gene symbol: EIF4E2
  hgvsc: ENST00000409167.3:c.219A>T
  hgvsp: ENSP00000387328.3:p.Glu73Asp
  variant of: http://identifiers.org/hgnc/3293
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28094
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7678
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6975
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11195
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1808
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu118Asp
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 311
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1008
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3296
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2404
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2015
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6365
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5668
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5812
bin: 9.75e1
variant carriers: 53

GenotypeQuality
all individuals: 13600
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4036
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 881
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 7.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2752
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6086
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.836074872376631e-4
allele num: 3526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 33
allele frequency: 1.020850089711068e-3
allele num: 32326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4340
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.75e-1

QD
type: SiteQuality
SIO_000300: 1.873e1

MQRankSum
type: SiteQuality
SIO_000300: -1.026e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQ
type: SiteQuality
SIO_000300: 5.554e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.87e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-2

DP
type: SiteQuality
SIO_000300: 1.36907e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

GenotypeQuality
all individuals: 1005
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12962
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 348
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1813
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4033
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5815
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3291
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10230
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6852
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2408
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 314
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5811
bin: 9.75e1
variant carriers: 53

GenotypeQuality
all individuals: 128
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.86368843069874e-4
allele num: 3492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6036
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4292
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2702
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 1.001564945226917e-3
allele num: 31950
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.485e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

VQSLOD
type: SiteQuality
SIO_000300: -5.923e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.58e-1

QD
type: SiteQuality
SIO_000300: 1.868e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-2

DP
type: SiteQuality
SIO_000300: 1.368395e6

GenotypeQuality
all individuals: 2408
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1717
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10858
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5766
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9510
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 9045
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3017
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3938
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3230
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3920
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.367388e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.069e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.12e-2

QD
type: SiteQuality
SIO_000300: 3.112e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 188
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2848
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1678
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2493
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2069
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2288
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41300
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524111443028714e-5
allele num: 65612
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: 862
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-2

FS
type: SiteQuality
SIO_000300: 1.991e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

QD
type: SiteQuality
SIO_000300: 1.477e1

DP
type: SiteQuality
SIO_000300: 3.125683e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.602e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.88e-1

GenotypeQuality
all individuals: 2402
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 211
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 194
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2846
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2492
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2068
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41301
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524576167825345e-5
allele num: 65592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13878
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.107e0

FS
type: SiteQuality
SIO_000300: 5.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.274e0

DP
type: SiteQuality
SIO_000300: 3.126615e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.901e0

QD
type: SiteQuality
SIO_000300: 1.121e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
all individuals: 177
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2491
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41299
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2847
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1681
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2494
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
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: 862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13910
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.092485549132948e-4
allele num: 8650
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 3.127434e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.093e0

MQRankSum
type: SiteQuality
SIO_000300: -1.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 1.123e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.02e-1

GenotypeQuality
all individuals: 152
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2587
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2847
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1697
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41298
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 258
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2072
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1110
bin: 7.25e1
variant carriers: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.141836880445651e-5
allele num: 14002
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.31e1

MQ
type: SiteQuality
SIO_000300: 5.947e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.7e-2

FS
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.33e-1

DP
type: SiteQuality
SIO_000300: 3.126697e6

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.5e0
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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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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521838380763963e-5
allele num: 65710
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14234
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

QD
type: SiteQuality
SIO_000300: 1.358e1

VQSLOD
type: SiteQuality
SIO_000300: 7.07e-1

FS
type: SiteQuality
SIO_000300: 5.9e-1

DP
type: SiteQuality
SIO_000300: 3.133809e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.393e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.44e-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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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14462
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65812
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.152073732718894e-3
allele num: 868
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

QD
type: SiteQuality
SIO_000300: 1.539e1

MQ
type: SiteQuality
SIO_000300: 5.941e1

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 3.139948e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.141e0

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
all individuals: 1133
bin: 7.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.928640308582449e-4
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65876
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: 14516
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.220000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.042e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

FS
type: SiteQuality
SIO_000300: 2.555e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.45e-1

DP
type: SiteQuality
SIO_000300: 3.144344e6

GenotypeQuality
all individuals: 2849
bin: 9.25e1
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
all individuals: 491
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65896
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.641342074816814e-5
allele num: 10372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.945e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.72e0

QD
type: SiteQuality
SIO_000300: 1.32e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

FS
type: SiteQuality
SIO_000300: 5.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.91e-1

DP
type: SiteQuality
SIO_000300: 3.145017e6

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.635767970707265e-5
allele num: 10378
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.329787234042553e-4
allele num: 15040
num of homozygotes: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 6.934812760055479e-4
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
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: 3
allele frequency: 4.541601065762383e-5
allele num: 66056
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.15e-1

DP
type: SiteQuality
SIO_000300: 3.155096e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.56e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.396e1

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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bin: 4.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66418
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.196e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.298e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-2

DP
type: SiteQuality
SIO_000300: 3.173811e6

QD
type: SiteQuality
SIO_000300: 1.433e1

FS
type: SiteQuality
SIO_000300: 1.839e0

MQRankSum
type: SiteQuality
SIO_000300: -1.766e0

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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bin: 6.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16134
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
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allele num: 904
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MQRankSum
type: SiteQuality
SIO_000300: 2.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

FS
type: SiteQuality
SIO_000300: 5.76e-1

DP
type: SiteQuality
SIO_000300: 3.179327e6

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.08e-1

QD
type: SiteQuality
SIO_000300: 1.219e1

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
all individuals: 48
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.591121091725686e-4
allele num: 11578
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16134
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 25
allele frequency: 3.759511564257572e-4
allele num: 66498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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QD
type: SiteQuality
SIO_000300: 1.219e1

FS
type: SiteQuality
SIO_000300: 5.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.179327e6

MQRankSum
type: SiteQuality
SIO_000300: 2.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.21e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeQuality
all individuals: 1172
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2512
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2859
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1517
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66510
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: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16192
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

DP
type: SiteQuality
SIO_000300: 3.175771e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.94e-1

FS
type: SiteQuality
SIO_000300: 8.702e0

VQSLOD
type: SiteQuality
SIO_000300: -1.067e-1

QD
type: SiteQuality
SIO_000300: 1.317e1

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1970
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1516
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.882952142994427e-4
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66526
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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16208
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.55e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

FS
type: SiteQuality
SIO_000300: 1.125e0

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.64e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.476e0

DP
type: SiteQuality
SIO_000300: 3.17631e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.56e-1

GenotypeQuality
all individuals: 6864
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2859
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2510
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502223290469895e-5
allele num: 66568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16310
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 3.177876e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.164e0

MQRankSum
type: SiteQuality
SIO_000300: 9.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

FS
type: SiteQuality
SIO_000300: 4.722e0

QD
type: SiteQuality
SIO_000300: 1.322e1

MQ
type: SiteQuality
SIO_000300: 5.989e1

VQSLOD
type: SiteQuality
SIO_000300: 2.91e-1

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

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 2000
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 24
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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
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 2860
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variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.591121091725686e-4
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16350
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 3.179026e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

QD
type: SiteQuality
SIO_000300: 1.325e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.206e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.99e-1

GenotypeQuality
all individuals: 1515
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 2862
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 7.44e0

FS
type: SiteQuality
SIO_000300: 1.519e0

DP
type: SiteQuality
SIO_000300: 3.180325e6

MQRankSum
type: SiteQuality
SIO_000300: -1.434e0

QD
type: SiteQuality
SIO_000300: 1.512e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.989e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.86e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

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

GenotypeQuality
all individuals: 1183
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2006
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1515
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 2119
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41288
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 2510
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

East Asian
type: Population
allele count: 13
allele frequency: 1.502195516524151e-3
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.44e-1

DP
type: SiteQuality
SIO_000300: 3.180338e6

FS
type: SiteQuality
SIO_000300: 1.384e0

MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.483e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.22e0

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

GenotypeQuality
all individuals: 1516
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 3
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GenotypeQuality
all individuals: 41284
bin: 9.75e1
variant carriers: 2

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e0

MQRankSum
type: SiteQuality
SIO_000300: 1.59e0

VQSLOD
type: SiteQuality
SIO_000300: -8.964e-1

QD
type: SiteQuality
SIO_000300: 1.581e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.179469e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.48e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 2128
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.319e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.491e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.59e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.52e-1

FS
type: SiteQuality
SIO_000300: 6.583e0

DP
type: SiteQuality
SIO_000300: 3.17963e6

QD
type: SiteQuality
SIO_000300: 1.351e1

VQSLOD
type: SiteQuality
SIO_000300: 7.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 1179
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variant carriers: 0

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 2859
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 1517
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41283
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7093
bin: 6.25e1
variant carriers: 0

South Asian
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African
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allele frequency: 9.609840476648087e-5
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num of homozygotes: 0

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

African
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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East Asian
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allele num: 8654
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South Asian
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: 4.51e-1

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66682
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African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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allele num: 16462
num of homozygotes: 0

Other
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num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.067e0

BaseQRankSum
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MQRankSum
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DP
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SIO_000300: 3.179269e6

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
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QD
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

Other
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allele num: 908
num of homozygotes: 0

African
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allele frequency: 9.609840476648087e-5
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num of homozygotes: 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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num of homozygotes: 0

MQRankSum
type: SiteQuality
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DP
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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FS
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MQ
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: 9.81e-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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variant carriers: 0

East Asian
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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East Asian
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South Asian
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European (Finnish)
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Latino
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Other
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ClippingRankSum
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MQ
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DP
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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

Other
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num of homozygotes: 0

European (Finnish)
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South Asian
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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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FS
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ReadPosRankSum
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InbreedingCoeff
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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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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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bin: 3.25e1
variant carriers: 0

African
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num of homozygotes: 0

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

European (Non-Finnish)
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Other
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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: 1.727712508638562e-4
allele num: 11576
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BaseQRankSum
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MQRankSum
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DP
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MQ
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ClippingRankSum
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ReadPosRankSum
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FS
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QD
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InbreedingCoeff
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VQSLOD
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SIO_000300: 3.12e-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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Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
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allele frequency: 4.872700694359849e-4
allele num: 16418
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 4.505992970650966e-5
allele num: 66578
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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 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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MQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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DP
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ClippingRankSum
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MQ
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InbreedingCoeff
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.503307276007216e-5
allele num: 66520
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African
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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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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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.023370678231538e-5
allele num: 66408
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
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Other
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QD
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ReadPosRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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FS
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DP
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VQSLOD
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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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

Other
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.204819277108434e-4
allele num: 66400
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East Asian
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South Asian
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FS
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MQ
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QD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

East Asian
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European (Non-Finnish)
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allele num: 66358
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South Asian
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Other
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European (Finnish)
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Latino
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DP
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ClippingRankSum
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VQSLOD
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FS
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BaseQRankSum
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MQRankSum
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QD
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ReadPosRankSum
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MQ
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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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variant carriers: 0

African
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allele num: 10400
num of homozygotes: 0

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

African
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East Asian
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Other
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European (Non-Finnish)
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allele num: 66318
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Latino
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South Asian
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BaseQRankSum
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VQSLOD
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FS
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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DP
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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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variant carriers: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15300
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.508614187007815e-5
allele num: 66286
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -5.372e0

VQSLOD
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

QD
type: SiteQuality
SIO_000300: 1.214e1

MQ
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SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 3.133655e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.52e-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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variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.613756613756614e-5
allele num: 15120
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66238
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 4.4e-3

QD
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BaseQRankSum
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SIO_000300: 8.799999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.41e-1

FS
type: SiteQuality
SIO_000300: 4.906e0

MQRankSum
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SIO_000300: -8.090000000000001e-1

MQ
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DP
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VQSLOD
type: SiteQuality
SIO_000300: -1.849e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.16e-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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.5355587808418e-5
allele num: 66144
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14794
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
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Other
type: Population
allele count: 0
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.96e-1

MQRankSum
type: SiteQuality
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DP
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SIO_000300: 3.122634e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 3
allele frequency: 4.538303279680504e-5
allele num: 66104
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
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African
type: Population
allele count: 2
allele frequency: 1.92492781520693e-4
allele num: 10390
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: 14662
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
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DP
type: SiteQuality
SIO_000300: 3.120528e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.147e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

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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variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14662
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512767759893501e-5
allele num: 66104
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-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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variant carriers: 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: 6614
num of homozygotes: 0

African
type: Population
allele count: 26
allele frequency: 2.502406159769009e-3
allele num: 10390
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66126
num of homozygotes: 0

East Asian
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FS
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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allele num: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 5.189413596263622e-4
allele num: 11562
num of homozygotes: 0

African
type: Population
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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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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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FS
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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East Asian
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South Asian
type: Population
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allele frequency: 7.095217823187172e-5
allele num: 14094
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African
type: Population
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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QD
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11148
num of homozygotes: 0

South Asian
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
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European (Finnish)
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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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African
type: Population
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Other
type: Population
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num of homozygotes: 0

BaseQRankSum
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MQ
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MQRankSum
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ClippingRankSum
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DP
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VQSLOD
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FS
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ReadPosRankSum
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InbreedingCoeff
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QD
type: SiteQuality
SIO_000300: 1.446e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3320
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.532e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.02e-2

DP
type: SiteQuality
SIO_000300: 6.36079e5

MQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

GenotypeQuality
all individuals: 13386
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3113
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7862
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.40691e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.92e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.04e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.677e0

MQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.527e1

GenotypeQuality
all individuals: 178
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1098
bin: 3.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 2

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1014
bin: 6.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3913
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7922
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.104e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 6.929999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.37e-2

DP
type: SiteQuality
SIO_000300: 6.61353e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 2.025e1

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7924
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 684
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1442
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.38e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

DP
type: SiteQuality
SIO_000300: 6.66284e5

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 2.723e1

GenotypeQuality
all individuals: 127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2895
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
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variant carriers: 0

GenotypeQuality
all individuals: 1036
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20175
bin: 7.5e0
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GenotypeQuality
all individuals: 384
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variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.25e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3394
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 1.336898395721925e-3
allele num: 1496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7972
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.24e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-2

FS
type: SiteQuality
SIO_000300: 4.251e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.01e-1

DP
type: SiteQuality
SIO_000300: 6.74675e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.23e0

QD
type: SiteQuality
SIO_000300: 6.74e0

GenotypeQuality
all individuals: 442
bin: 5.75e1
variant carriers: 406

GenotypeQuality
all individuals: 11220
bin: 2.25e1
variant carriers: 1128

GenotypeQuality
all individuals: 3499
bin: 6.25e1
variant carriers: 684

GenotypeQuality
all individuals: 346
bin: 8.75e1
variant carriers: 283

GenotypeQuality
all individuals: 2563
bin: 1.25e1
variant carriers: 691

GenotypeQuality
all individuals: 483
bin: 3.75e1
variant carriers: 260

GenotypeQuality
all individuals: 191
bin: 4.25e1
variant carriers: 107

GenotypeQuality
all individuals: 6113
bin: 2.5e0
variant carriers: 18

GenotypeQuality
all individuals: 1320
bin: 6.75e1
variant carriers: 652

GenotypeQuality
all individuals: 625
bin: 9.25e1
variant carriers: 543

GenotypeQuality
all individuals: 761
bin: 7.25e1
variant carriers: 534

GenotypeQuality
all individuals: 1280
bin: 3.25e1
variant carriers: 789

Other
type: Population
allele count: 93
allele frequency: 3.444444444444444e-1
allele num: 270
num of homozygotes: 11

European (Non-Finnish)
type: Population
allele count: 4972
allele frequency: 3.312017053024247e-1
allele num: 15012
num of homozygotes: 671

European (Finnish)
type: Population
allele count: 297
allele frequency: 4.21875e-1
allele num: 704
num of homozygotes: 33

South Asian
type: Population
allele count: 2096
allele frequency: 2.482235907153008e-1
allele num: 8444
num of homozygotes: 247

African
type: Population
allele count: 1893
allele frequency: 4.447838345864661e-1
allele num: 4256
num of homozygotes: 391

Latino
type: Population
allele count: 993
allele frequency: 5.807017543859649e-1
allele num: 1710
num of homozygotes: 231

East Asian
type: Population
allele count: 902
allele frequency: 3.857998289136014e-1
allele num: 2338
num of homozygotes: 126

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.68e-1

QD
type: SiteQuality
SIO_000300: 1.852e1

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

FS
type: SiteQuality
SIO_000300: 6.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.964e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 7.82241e5

GenotypeQuality
all individuals: 472
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 191
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
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variant carriers: 0

GenotypeQuality
all individuals: 2563
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 625
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variant carriers: 0

GenotypeQuality
all individuals: 442
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variant carriers: 1

GenotypeQuality
all individuals: 3499
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 11951
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1280
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.998401278976818e-4
allele num: 15012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1710
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

DP
type: SiteQuality
SIO_000300: 7.82241e5

FS
type: SiteQuality
SIO_000300: 6.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.964e-1

QD
type: SiteQuality
SIO_000300: 1.852e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

GenotypeQuality
all individuals: 3499
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 11951
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
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variant carriers: 0

GenotypeQuality
all individuals: 200
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GenotypeQuality
all individuals: 625
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variant carriers: 0

GenotypeQuality
all individuals: 346
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GenotypeQuality
all individuals: 11220
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
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variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2338
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.68e-1

QD
type: SiteQuality
SIO_000300: 1.852e1

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

DP
type: SiteQuality
SIO_000300: 7.82241e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.964e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

FS
type: SiteQuality
SIO_000300: 6.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
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GenotypeQuality
all individuals: 2305
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GenotypeQuality
all individuals: 1911
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GenotypeQuality
all individuals: 25781
bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 944
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GenotypeQuality
all individuals: 2426
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variant carriers: 0

GenotypeQuality
all individuals: 505
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GenotypeQuality
all individuals: 152
bin: 8.75e1
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GenotypeQuality
all individuals: 535
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variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1740
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 692
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15742
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4388
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.89e-1

QD
type: SiteQuality
SIO_000300: 2.298e1

VQSLOD
type: SiteQuality
SIO_000300: -1.141e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

FS
type: SiteQuality
SIO_000300: 7.574e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.24e-2

DP
type: SiteQuality
SIO_000300: 7.09901e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.629e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

GenotypeQuality
all individuals: 1736
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 8.75e1
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GenotypeQuality
all individuals: 26575
bin: 2.25e1
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GenotypeQuality
all individuals: 923
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GenotypeQuality
all individuals: 343
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
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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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bin: 9.75e1
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 count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1748
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 15798
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 274
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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4390
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.166e0

DP
type: SiteQuality
SIO_000300: 7.15859e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.23e-2

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.93e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.112e0

GenotypeQuality
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bin: 6.75e1
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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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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 17506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1904
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.127141568981064e-4
allele num: 8872
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3006
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4686
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.177e1

FS
type: SiteQuality
SIO_000300: 5.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
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DP
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VQSLOD
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SIO_000300: 3.03e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

GenotypeQuality
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variant carriers: 2

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

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 2

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3006
num of homozygotes: 0

African
type: Population
allele count: 78
allele frequency: 1.664532650448143e-2
allele num: 4686
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 17506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8872
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1904
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.69e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.63157e5

InbreedingCoeff
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SIO_000300: 1.48e-2

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.789e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.177e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8964
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18116
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3168
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 5.0e-4
allele num: 2000
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.51e-2

QD
type: SiteQuality
SIO_000300: 8.390000000000001e0

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.84e-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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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.219765381044814e-5
allele num: 23698
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9698
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3106
num of homozygotes: 0

African
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: 384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4214
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.72e-1

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

DP
type: SiteQuality
SIO_000300: 8.71312e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.299999999999999e-3

FS
type: SiteQuality
SIO_000300: 6.996e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-1

QD
type: SiteQuality
SIO_000300: 1.201e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3234
num of homozygotes: 0

African
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: 388
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.090648776896016e-5
allele num: 24446
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 8.77464e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.29e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.068348250610252e-5
allele num: 24580
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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
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VQSLOD
type: SiteQuality
SIO_000300: 2.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.44e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 8.79384e5

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.31e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

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

Latino
type: Population
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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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East Asian
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allele frequency: 2.325581395348837e-4
allele num: 4300
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 24774
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South Asian
type: Population
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -9.4e-3

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.986e1

DP
type: SiteQuality
SIO_000300: 8.79271e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

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

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

African
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allele frequency: 1.789549033643522e-4
allele num: 5588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3312
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -9.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

DP
type: SiteQuality
SIO_000300: 8.78642e5

GenotypeQuality
all individuals: 180
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1425
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4712
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11250
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 344
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2289
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32915
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5528
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 8.21422704123542e-5
allele num: 24348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

DP
type: SiteQuality
SIO_000300: 8.64156e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.775e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

FS
type: SiteQuality
SIO_000300: 2.401e0

QD
type: SiteQuality
SIO_000300: 2.91e0

VQSLOD
type: SiteQuality
SIO_000300: -2.618e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

GenotypeQuality
all individuals: 180
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1425
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4712
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2289
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1728
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11250
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32915
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 152
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5528
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3222
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.10711352061771e-5
allele num: 24348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1428
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.91e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 8.64156e5

VQSLOD
type: SiteQuality
SIO_000300: -2.618e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.775e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

FS
type: SiteQuality
SIO_000300: 2.401e0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.05e-1

GenotypeQuality
all individuals: 339
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30664
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1549
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 497
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 3.25e1
variant carriers: 0