1-21167384-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167384
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167384
    reference: chr 1
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.3018G>A
  hgvsp: ENST00000374935.3:c.3018G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3876G>A
  hgvsp: ENST00000374937.3:c.3876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2670G>A
  hgvsp: ENST00000536266.1:c.2670G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2328G>A
  hgvsp: ENST00000537738.1:c.2328G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3876G>A
  hgvsp: ENST00000602326.1:c.3876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3858G>A
  hgvsp: ENST00000264211.8:c.3858G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3858G>A
  hgvsp: ENST00000400422.1:c.3858G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.278G>A
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1885
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln1292Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-21167401-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167401
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167401
    reference: chr 1
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3841C>T
  hgvsp: ENSP00000264211.7:p.Leu1281Phe
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2311C>T
  hgvsp: ENSP00000442010.1:p.Leu771Phe
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.261C>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2653C>T
  hgvsp: ENSP00000444693.1:p.Leu885Phe
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3841C>T
  hgvsp: ENSP00000383274.1:p.Leu1281Phe
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3859C>T
  hgvsp: ENSP00000364073.3:p.Leu1287Phe
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.3001C>T
  hgvsp: ENSP00000364071.3:p.Leu1001Phe
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3859C>T
  hgvsp: ENSP00000473510.1:p.Leu1287Phe
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3005
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu1287Phe
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

1-21167404-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167404
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167404
    reference: chr 1
allele count: 119363
allele frequency: 9.831235792178697e-1
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3856T>C
  hgvsp: ENST00000374937.3:c.3856T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2650T>C
  hgvsp: ENST00000536266.1:c.2650T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3856T>C
  hgvsp: ENST00000602326.1:c.3856T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3838T>C
  hgvsp: ENST00000400422.1:c.3838T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2308T>C
  hgvsp: ENST00000537738.1:c.2308T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3838T>C
  hgvsp: ENST00000264211.8:c.3838T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.258T>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2998T>C
  hgvsp: ENST00000374935.3:c.2998T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.75e1
  variant carriers: 581
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 7.75e1
  variant carriers: 3356
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 6.25e1
  variant carriers: 1726
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 3.75e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 6.75e1
  variant carriers: 2260
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 7.25e1
  variant carriers: 2825
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 304
genotype depth: GenotypeDepth
  all individuals: 34788
  bin: 9.75e1
  variant carriers: 34786
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.25e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 8.25e1
  variant carriers: 3860
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 5.75e1
  variant carriers: 1237
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 5.25e1
  variant carriers: 863
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 8.75e1
  variant carriers: 4121
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 9.25e1
  variant carriers: 4348
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.25e1
  variant carriers: 5
hgvs: p.Leu1286Leu
num of homozygotes: 58828
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

1-21167420-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167420
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167420
    reference: chr 1
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3822G>A
  hgvsp: ENST00000264211.8:c.3822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3840G>A
  hgvsp: ENST00000602326.1:c.3840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2292G>A
  hgvsp: ENST00000537738.1:c.2292G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2634G>A
  hgvsp: ENST00000536266.1:c.2634G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.242G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2982G>A
  hgvsp: ENST00000374935.3:c.2982G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3822G>A
  hgvsp: ENST00000400422.1:c.3822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3840G>A
  hgvsp: ENST00000374937.3:c.3840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3054
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg1280Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

1-21167430-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167430
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167430
    reference: chr 1
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3812A>G
  hgvsp: ENSP00000264211.7:p.Gln1271Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2624A>G
  hgvsp: ENSP00000444693.1:p.Gln875Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2282A>G
  hgvsp: ENSP00000442010.1:p.Gln761Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3830A>G
  hgvsp: ENSP00000364073.3:p.Gln1277Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2972A>G
  hgvsp: ENSP00000364071.3:p.Gln991Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3812A>G
  hgvsp: ENSP00000383274.1:p.Gln1271Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.232A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3830A>G
  hgvsp: ENSP00000473510.1:p.Gln1277Arg
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6160
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln1277Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

1-21167431-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167431
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167431
    reference: chr 1
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3811C>A
  hgvsp: ENSP00000383274.1:p.Gln1271Lys
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2971C>A
  hgvsp: ENSP00000364071.3:p.Gln991Lys
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3811C>A
  hgvsp: ENSP00000264211.7:p.Gln1271Lys
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3829C>A
  hgvsp: ENSP00000473510.1:p.Gln1277Lys
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2281C>A
  hgvsp: ENSP00000442010.1:p.Gln761Lys
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.231C>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3829C>A
  hgvsp: ENSP00000364073.3:p.Gln1277Lys
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2623C>A
  hgvsp: ENSP00000444693.1:p.Gln875Lys
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4250
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2891
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9830
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln1277Lys
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

1-21167434-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167434
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167434
    reference: chr 1
allele count: 5
allele frequency: 4.11834475487612e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3808A>C
  hgvsp: ENSP00000264211.7:p.Ser1270Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2620A>C
  hgvsp: ENSP00000444693.1:p.Ser874Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.228A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2968A>C
  hgvsp: ENSP00000364071.3:p.Ser990Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3808A>C
  hgvsp: ENSP00000383274.1:p.Ser1270Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3826A>C
  hgvsp: ENSP00000473510.1:p.Ser1276Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2278A>C
  hgvsp: ENSP00000442010.1:p.Ser760Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3826A>C
  hgvsp: ENSP00000364073.3:p.Ser1276Arg
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2891
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31527
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser1276Arg
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: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

1-21167448-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167448
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167448
    reference: chr 1
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.214C>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3794C>T
  hgvsp: ENSP00000264211.7:p.Ser1265Phe
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3812C>T
  hgvsp: ENSP00000473510.1:p.Ser1271Phe
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3812C>T
  hgvsp: ENSP00000364073.3:p.Ser1271Phe
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2606C>T
  hgvsp: ENSP00000444693.1:p.Ser869Phe
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3794C>T
  hgvsp: ENSP00000383274.1:p.Ser1265Phe
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2264C>T
  hgvsp: ENSP00000442010.1:p.Ser755Phe
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2954C>T
  hgvsp: ENSP00000364071.3:p.Ser985Phe
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7068
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2883
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4248
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser1271Phe
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

1-21167451-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167451
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167451
    reference: chr 1
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3791A>C
  hgvsp: ENSP00000264211.7:p.Glu1264Ala
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3791A>C
  hgvsp: ENSP00000383274.1:p.Glu1264Ala
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2603A>C
  hgvsp: ENSP00000444693.1:p.Glu868Ala
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3809A>C
  hgvsp: ENSP00000364073.3:p.Glu1270Ala
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2951A>C
  hgvsp: ENSP00000364071.3:p.Glu984Ala
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.211A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3809A>C
  hgvsp: ENSP00000473510.1:p.Glu1270Ala
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2261A>C
  hgvsp: ENSP00000442010.1:p.Glu754Ala
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu1270Ala
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

1-21167478-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167478
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167478
    reference: chr 1
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3782T>C
  hgvsp: ENSP00000364073.3:p.Leu1261Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3782T>C
  hgvsp: ENSP00000473510.1:p.Leu1261Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2234T>C
  hgvsp: ENSP00000442010.1:p.Leu745Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.184T>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3764T>C
  hgvsp: ENSP00000264211.7:p.Leu1255Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2576T>C
  hgvsp: ENSP00000444693.1:p.Leu859Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3764T>C
  hgvsp: ENSP00000383274.1:p.Leu1255Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2924T>C
  hgvsp: ENSP00000364071.3:p.Leu975Pro
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2878
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31590
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu1261Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

1-21167489-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167489
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167489
    reference: chr 1
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3771C>T
  hgvsp: ENST00000602326.1:c.3771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2565C>T
  hgvsp: ENST00000536266.1:c.2565C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2223C>T
  hgvsp: ENST00000537738.1:c.2223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.173C>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3771C>T
  hgvsp: ENST00000374937.3:c.3771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3753C>T
  hgvsp: ENST00000400422.1:c.3753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2913C>T
  hgvsp: ENST00000374935.3:c.2913C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3753C>T
  hgvsp: ENST00000264211.8:c.3753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31596
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala1257Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

1-21167499-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167499
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167499
    reference: chr 1
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2213A>T
  hgvsp: ENSP00000442010.1:p.Glu738Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3743A>T
  hgvsp: ENSP00000264211.7:p.Glu1248Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2903A>T
  hgvsp: ENSP00000364071.3:p.Glu968Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2555A>T
  hgvsp: ENSP00000444693.1:p.Glu852Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.163A>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3743A>T
  hgvsp: ENSP00000383274.1:p.Glu1248Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3761A>T
  hgvsp: ENSP00000364073.3:p.Glu1254Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3761A>T
  hgvsp: ENSP00000473510.1:p.Glu1254Val
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7041
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16776
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1734
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6112
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu1254Val
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

1-21167500-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167500
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167500
    reference: chr 1
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3760G>C
  hgvsp: ENSP00000364073.3:p.Glu1254Gln
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3760G>C
  hgvsp: ENSP00000473510.1:p.Glu1254Gln
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2902G>C
  hgvsp: ENSP00000364071.3:p.Glu968Gln
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2212G>C
  hgvsp: ENSP00000442010.1:p.Glu738Gln
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3742G>C
  hgvsp: ENSP00000264211.7:p.Glu1248Gln
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3742G>C
  hgvsp: ENSP00000383274.1:p.Glu1248Gln
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2554G>C
  hgvsp: ENSP00000444693.1:p.Glu852Gln
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.162G>C
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7041
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2865
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu1254Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

1-21167501-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167501
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167501
    reference: chr 1
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3741A>G
  hgvsp: ENST00000264211.8:c.3741A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2553A>G
  hgvsp: ENST00000536266.1:c.2553A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.161A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3759A>G
  hgvsp: ENST00000374937.3:c.3759A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2211A>G
  hgvsp: ENST00000537738.1:c.2211A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3741A>G
  hgvsp: ENST00000400422.1:c.3741A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3759A>G
  hgvsp: ENST00000602326.1:c.3759A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2901A>G
  hgvsp: ENST00000374935.3:c.2901A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7041
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1733
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3038
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2866
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu1253Glu
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

1-21167503-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167503
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167503
    reference: chr 1
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2209G>A
  hgvsp: ENSP00000442010.1:p.Glu737Lys
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3739G>A
  hgvsp: ENSP00000264211.7:p.Glu1247Lys
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2899G>A
  hgvsp: ENSP00000364071.3:p.Glu967Lys
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3757G>A
  hgvsp: ENSP00000364073.3:p.Glu1253Lys
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3739G>A
  hgvsp: ENSP00000383274.1:p.Glu1247Lys
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2551G>A
  hgvsp: ENSP00000444693.1:p.Glu851Lys
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3757G>A
  hgvsp: ENSP00000473510.1:p.Glu1253Lys
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.159G>A
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7039
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31596
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4221
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6104
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu1253Lys
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

1-21167515-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167515
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167515
    reference: chr 1
allele count: 2
allele frequency: 1.649321304283287e-5
allele num: 121262
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.147A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3727A>G
  hgvsp: ENSP00000383274.1:p.Met1243Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3745A>G
  hgvsp: ENSP00000364073.3:p.Met1249Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3727A>G
  hgvsp: ENSP00000264211.7:p.Met1243Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2539A>G
  hgvsp: ENSP00000444693.1:p.Met847Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3745A>G
  hgvsp: ENSP00000473510.1:p.Met1249Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2887A>G
  hgvsp: ENSP00000364071.3:p.Met963Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2197A>G
  hgvsp: ENSP00000442010.1:p.Met733Val
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met1249Val
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

1-21167516-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167516
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167516
    reference: chr 1
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3726C>T
  hgvsp: ENST00000264211.8:c.3726C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2196C>T
  hgvsp: ENST00000537738.1:c.2196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2886C>T
  hgvsp: ENST00000374935.3:c.2886C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3726C>T
  hgvsp: ENST00000400422.1:c.3726C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3744C>T
  hgvsp: ENST00000602326.1:c.3744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2538C>T
  hgvsp: ENST00000536266.1:c.2538C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.146C>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3744C>T
  hgvsp: ENST00000374937.3:c.3744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala1248Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

1-21167531-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167531
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167531
    reference: chr 1
allele count: 1
allele frequency: 8.265555775970376e-6
allele num: 120984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3721-10G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3739-10G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.141-10G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2533-10G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2881-10G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3721-10G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2191-10G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3739-10G>A
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2951
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6045
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS

1-21167542-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167542
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167542
    reference: chr 1
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.141-21C>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2191-21C>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3739-21C>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2881-21C>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3721-21C>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3739-21C>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2533-21C>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3721-21C>G
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15854
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6028
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4078
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2779
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

1-21167562-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167562
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167562
    reference: chr 1
allele count: 1
allele frequency: 8.320852055250457e-6
allele num: 120180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2191-41A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2533-41A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3739-41A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2881-41A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3739-41A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3721-41A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.141-41A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3721-41A>C
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7703
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7746
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2638
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2731
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

1-21167565-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167565
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167565
    reference: chr 1
allele count: 582
allele frequency: 4.848949394297902e-3
allele num: 120026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2881-44A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3721-44A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2191-44A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3739-44A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.141-44A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3739-44A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2533-44A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3721-44A>G
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8122
  bin: 1.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 4.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13994
  bin: 2.75e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 7342
  bin: 2.25e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 3.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 4.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12043
  bin: 3.25e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1660
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3634
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2043
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18521
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 10
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

1-21167565-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21167565
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21167565
    reference: chr 1
allele count: 1
allele frequency: 8.33152816889674e-6
allele num: 120026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2881-44A>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2191-44A>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3739-44A>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.141-44A>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3721-44A>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3721-44A>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2533-44A>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3739-44A>T
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13994
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2739
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7248
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18521
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3856
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

1-21174250-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21174250
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21174251
    reference: chr 1
allele count: 1
allele frequency: 5.453752181500873e-5
allele num: 18336
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+1657dupA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+1657dupA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+1657dupA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+1657dupA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.140+48dupA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+1657dupA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+1657dupA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+1657dupA
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 939
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3743
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-21174283-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21174283
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21174283
    reference: chr 1
allele count: 1
allele frequency: 5.448403617740002e-5
allele num: 18354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+1625A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+1625A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+1625A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+1625A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.140+16A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+1625A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+1625A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+1625A>G
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1087
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

1-21174316-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21174316
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21174316
    reference: chr 1
allele count: 1
allele frequency: 5.471656817684395e-5
allele num: 18276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+1592A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+1592A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+1592A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+1592A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.123A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+1592A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+1592A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+1592A>G
  variant of: http://identifiers.org/hgnc/3298
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3740
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/1-21174336-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21174336
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21174336
    reference: chr 1
allele count: 1
allele frequency: 5.513287021722351e-5
allele num: 18138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.103G>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+1572G>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+1572G>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+1572G>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+1572G>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+1572G>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+1572G>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+1572G>T
  variant of: http://identifiers.org/hgnc/3298
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-21174353-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21174353
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21174353
    reference: chr 1
allele count: 1
allele frequency: 5.55926173004225e-5
allele num: 17988
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+1555T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+1555T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+1555T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075151
  ensembl transcript: ENST00000435383
  gene symbol: EIF4G3
  hgvsc: ENST00000435383.1:n.86T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+1555T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+1555T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+1555T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+1555T>G
  variant of: http://identifiers.org/hgnc/3298
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD

1-21175858-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175858
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175858
    reference: chr 1
allele count: 1
allele frequency: 1.148237455505799e-5
allele num: 87090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+50A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+50A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+50A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+50A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+50A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+50A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+50A>G
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19586
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14099
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11925
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3672
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5283
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4261
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1643
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4493
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11347
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7919
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

1-21175861-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175861
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175861
    reference: chr 1
allele count: 1
allele frequency: 1.145475372279496e-5
allele num: 87300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+47A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+47A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+47A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+47A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+47A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+47A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+47A>G
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19537
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14017
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11032
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1983
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1754
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6526
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4093
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7887
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2740
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-21175869-GACTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175869
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175865
    reference: chr 1
allele count: 66
allele frequency: 7.440643953913102e-4
allele num: 88702
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+35_2880+38delAAGT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+35_2532+38delAAGT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+35_3720+38delAAGT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+35_2190+38delAAGT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+35_3738+38delAAGT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+35_3720+38delAAGT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+35_3738+38delAAGT
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18623
  bin: 1.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10421
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7624
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 13734
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1215
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14340
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2160
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5231
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 3
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: GACTT
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

1-21175875-CTGTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175875
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175871
    reference: chr 1
allele count: 46
allele frequency: 5.157991522953062e-4
allele num: 89182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+29_2190+32delCACA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+29_3720+32delCACA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+29_3738+32delCACA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+29_3720+32delCACA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+29_2880+32delCACA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+29_3738+32delCACA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+29_2532+32delCACA
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5834
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16329
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13152
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14362
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4609
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1375
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2246
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4927
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1487
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: CTGTG
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

1-21175875-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175875
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175873
    reference: chr 1
allele count: 5
allele frequency: 5.606512524948981e-5
allele num: 89182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+31_3720+32delCA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+31_2190+32delCA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+31_2880+32delCA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+31_3720+32delCA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+31_3738+32delCA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+31_2532+32delCA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+31_3738+32delCA
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14362
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5834
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14088
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2246
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1487
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4609
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: CTG
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

1-21175883-GTGT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175883
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175880
    reference: chr 1
allele count: 8
allele frequency: 8.443271767810026e-5
allele num: 94750
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+22_3720+24delACA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+22_3738+24delACA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+22_3738+24delACA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+22_2880+24delACA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+22_2532+24delACA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+22_2190+24delACA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+22_3720+24delACA
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12316
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6243
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19158
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2966
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4150
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5148
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 882
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: GTGT
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP

1-21175884-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175884
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175884
    reference: chr 1
allele count: 1
allele frequency: 1.057887610020311e-5
allele num: 94528
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+24A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+24A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+24A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+24A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+24A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+24A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+24A>G
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11992
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10981
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18726
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1111
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13105
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5032
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

1-21175885-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175885
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175886
    reference: chr 1
allele count: 503
allele frequency: 9.407847978154341e-3
allele num: 53466
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+22dupA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+22dupA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+22dupA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+22dupA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+22dupA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+22dupA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+22dupA
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 3.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8196
  bin: 1.25e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 9864
  bin: 2.75e1
  variant carriers: 146
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14161
  bin: 2.25e1
  variant carriers: 237
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 7.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9504
  bin: 1.75e1
  variant carriers: 236
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 7029
  bin: 2.25e1
  variant carriers: 87
genotype quality: GenotypeQuality
  all individuals: 20679
  bin: 2.5e0
  variant carriers: 59
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 5.25e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 1611
  bin: 4.25e1
  variant carriers: 53
genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 9.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 2414
  bin: 3.75e1
  variant carriers: 65
genotype quality: GenotypeQuality
  all individuals: 2683
  bin: 1.75e1
  variant carriers: 92
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 7.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3316
  bin: 2.75e1
  variant carriers: 78
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

1-21175885-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175885
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175885
    reference: chr 1
allele count: 1
allele frequency: 1.870347510567463e-5
allele num: 53466
alternate allele: T
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14161
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6629
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3267
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2683
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7029
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2414
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1611
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3316
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20679
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2934
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3316
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 9.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4228
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 3.365870077415012e-5
  allele num: 29710
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 440
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4930
  num of homozygotes: 0
population: Latino
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

1-21175885-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175885
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175884
    reference: chr 1
allele count: 2520
allele frequency: 4.713275726630008e-2
allele num: 53466
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+22delA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+22delA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+22delA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+22delA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+22delA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+22delA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+22delA
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 8196
  bin: 1.25e1
  variant carriers: 160
genotype depth: GenotypeDepth
  all individuals: 14161
  bin: 2.25e1
  variant carriers: 945
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 3.25e1
  variant carriers: 288
genotype depth: GenotypeDepth
  all individuals: 9864
  bin: 2.75e1
  variant carriers: 833
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 7.5e0
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 3.75e1
  variant carriers: 149
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 9504
  bin: 1.75e1
  variant carriers: 573
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 9.75e1
  variant carriers: 282
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 4.75e1
  variant carriers: 142
genotype quality: GenotypeQuality
  all individuals: 2934
  bin: 1.25e1
  variant carriers: 294
genotype quality: GenotypeQuality
  all individuals: 20679
  bin: 2.5e0
  variant carriers: 216
genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 9.75e1
  variant carriers: 559
genotype quality: GenotypeQuality
  all individuals: 2683
  bin: 1.75e1
  variant carriers: 312
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 8.25e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 1611
  bin: 4.25e1
  variant carriers: 174
genotype quality: GenotypeQuality
  all individuals: 3316
  bin: 2.75e1
  variant carriers: 302
genotype quality: GenotypeQuality
  all individuals: 3316
  bin: 7.5e0
  variant carriers: 308
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 5.25e1
  variant carriers: 120
num of homozygotes: 6
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: GT
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

1-21175885-GTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175885
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175883
    reference: chr 1
allele count: 3
allele frequency: 5.611042531702391e-5
allele num: 53466
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+21_2532+22delAA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+21_3738+22delAA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+21_3720+22delAA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+21_2880+22delAA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+21_3738+22delAA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+21_3720+22delAA
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+21_2190+22delAA
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9504
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8196
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3316
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2934
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6629
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2683
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20679
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: GTT
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum

1-21175885-GTTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175885
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175882
    reference: chr 1
allele count: 1
allele frequency: 1.870347510567463e-5
allele num: 53466
alternate allele: G
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9504
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7029
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2934
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3316
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1611
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6629
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20679
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2414
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3316
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2683
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3267
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4228
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5496
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 440
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3854
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: GTTT
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

1-21175886-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175886
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175886
    reference: chr 1
allele count: 6
allele frequency: 1.145562853215213e-4
allele num: 52376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+22A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+22A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+22A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+22A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+22A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+22A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+22A>C
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13039
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9069
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7142
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1372
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17413
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3117
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3862
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum

1-21175886-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175886
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175887
    reference: chr 1
allele count: 42
allele frequency: 8.018939972506492e-4
allele num: 52376
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+21_2532+22insC
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+21_2880+22insC
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+21_3720+22insC
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+21_2190+22insC
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+21_3720+22insC
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+21_3738+22insC
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+21_3738+22insC
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9069
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9123
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13039
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 17413
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3435
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3862
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2561
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

1-21175886-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175886
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175886
    reference: chr 1
allele count: 1
allele frequency: 1.909271422025355e-5
allele num: 52376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+22A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+22A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+22A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+22A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+22A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+22A>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+22A>G
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9069
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13039
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1372
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2561
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3117
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7881
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1187
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17413
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD

1-21175887-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175887
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175887
    reference: chr 1
allele count: 5
allele frequency: 6.854761317210935e-5
allele num: 72942
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3738+21A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3720+21A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2190+21A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2880+21A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3720+21A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3738+21A>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2532+21A>C
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6006
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9411
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13998
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2112
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10267
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12913
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3127
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3903
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3902
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1759
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-21175920-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175920
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175920
    reference: chr 1
allele count: 1
allele frequency: 8.448514751106756e-6
allele num: 118364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2520T>G
  hgvsp: ENSP00000444693.1:p.Ile840Met
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3726T>G
  hgvsp: ENSP00000473510.1:p.Ile1242Met
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2868T>G
  hgvsp: ENSP00000364071.3:p.Ile956Met
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3708T>G
  hgvsp: ENSP00000264211.7:p.Ile1236Met
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2178T>G
  hgvsp: ENSP00000442010.1:p.Ile726Met
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3708T>G
  hgvsp: ENSP00000383274.1:p.Ile1236Met
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3726T>G
  hgvsp: ENSP00000364073.3:p.Ile1242Met
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1663
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1923
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1667
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile1242Met
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

1-21175923-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175923
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175923
    reference: chr 1
allele count: 2
allele frequency: 1.683331650001683e-5
allele num: 118812
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2517C>T
  hgvsp: ENST00000536266.1:c.2517C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2175C>T
  hgvsp: ENST00000537738.1:c.2175C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2865C>T
  hgvsp: ENST00000374935.3:c.2865C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3705C>T
  hgvsp: ENST00000264211.8:c.3705C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3705C>T
  hgvsp: ENST00000400422.1:c.3705C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3723C>T
  hgvsp: ENST00000374937.3:c.3723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3723C>T
  hgvsp: ENST00000602326.1:c.3723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15668
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6851
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1924
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His1241His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS

1-21175943-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175943
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175943
    reference: chr 1
allele count: 1
allele frequency: 8.305647840531562e-6
allele num: 120400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2845A>G
  hgvsp: ENSP00000364071.3:p.Ile949Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3703A>G
  hgvsp: ENSP00000473510.1:p.Ile1235Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2497A>G
  hgvsp: ENSP00000444693.1:p.Ile833Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3703A>G
  hgvsp: ENSP00000364073.3:p.Ile1235Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2155A>G
  hgvsp: ENSP00000442010.1:p.Ile719Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3685A>G
  hgvsp: ENSP00000383274.1:p.Ile1229Val
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3685A>G
  hgvsp: ENSP00000264211.7:p.Ile1229Val
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7577
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30112
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6976
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile1235Val
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

1-21175953-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175953
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175953
    reference: chr 1
allele count: 1
allele frequency: 8.286377195889957e-6
allele num: 120680
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2145G>A
  hgvsp: ENST00000537738.1:c.2145G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3693G>A
  hgvsp: ENST00000374937.3:c.3693G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2835G>A
  hgvsp: ENST00000374935.3:c.2835G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3675G>A
  hgvsp: ENST00000400422.1:c.3675G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3675G>A
  hgvsp: ENST00000264211.8:c.3675G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2487G>A
  hgvsp: ENST00000536266.1:c.2487G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3693G>A
  hgvsp: ENST00000602326.1:c.3693G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46582
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys1231Lys
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-21175954-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175954
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175954
    reference: chr 1
allele count: 1
allele frequency: 8.284317786430287e-6
allele num: 120710
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3674A>G
  hgvsp: ENSP00000383274.1:p.Lys1225Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2144A>G
  hgvsp: ENSP00000442010.1:p.Lys715Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2486A>G
  hgvsp: ENSP00000444693.1:p.Lys829Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3692A>G
  hgvsp: ENSP00000473510.1:p.Lys1231Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2834A>G
  hgvsp: ENSP00000364071.3:p.Lys945Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3692A>G
  hgvsp: ENSP00000364073.3:p.Lys1231Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3674A>G
  hgvsp: ENSP00000264211.7:p.Lys1225Arg
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7020
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys1231Arg
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum

1-21175955-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175955
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175955
    reference: chr 1
allele count: 13
allele frequency: 1.076782904000663e-4
allele num: 120730
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2143A>G
  hgvsp: ENSP00000442010.1:p.Lys715Glu
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3691A>G
  hgvsp: ENSP00000364073.3:p.Lys1231Glu
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3673A>G
  hgvsp: ENSP00000264211.7:p.Lys1225Glu
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2485A>G
  hgvsp: ENSP00000444693.1:p.Lys829Glu
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2833A>G
  hgvsp: ENSP00000364071.3:p.Lys945Glu
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3673A>G
  hgvsp: ENSP00000383274.1:p.Lys1225Glu
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3691A>G
  hgvsp: ENSP00000473510.1:p.Lys1231Glu
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30220
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16597
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1933
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys1231Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/1-21175968-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175968
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175968
    reference: chr 1
allele count: 19
allele frequency: 1.571910781653319e-4
allele num: 120872
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3678G>T
  hgvsp: ENSP00000473510.1:p.Glu1226Asp
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2130G>T
  hgvsp: ENSP00000442010.1:p.Glu710Asp
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2820G>T
  hgvsp: ENSP00000364071.3:p.Glu940Asp
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3678G>T
  hgvsp: ENSP00000364073.3:p.Glu1226Asp
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3660G>T
  hgvsp: ENSP00000383274.1:p.Glu1220Asp
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2472G>T
  hgvsp: ENSP00000444693.1:p.Glu824Asp
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3660G>T
  hgvsp: ENSP00000264211.7:p.Glu1220Asp
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16735
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1950
  bin: 9.75e1
  variant carriers: 18
hgvs: p.Glu1226Asp
num of homozygotes: 1
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-21175968-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175968
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175968
    reference: chr 1
allele count: 13
allele frequency: 1.075517903236482e-4
allele num: 120872
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2472G>A
  hgvsp: ENST00000536266.1:c.2472G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2820G>A
  hgvsp: ENST00000374935.3:c.2820G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2130G>A
  hgvsp: ENST00000537738.1:c.2130G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3660G>A
  hgvsp: ENST00000264211.8:c.3660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3660G>A
  hgvsp: ENST00000400422.1:c.3660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3678G>A
  hgvsp: ENST00000374937.3:c.3678G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3678G>A
  hgvsp: ENST00000602326.1:c.3678G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30202
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1461
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46760
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu1226Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-21175985-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175985
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175985
    reference: chr 1
allele count: 2
allele frequency: 1.65508109897385e-5
allele num: 120840
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3661G>T
  hgvsp: ENSP00000473510.1:p.Ala1221Ser
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3661G>T
  hgvsp: ENSP00000364073.3:p.Ala1221Ser
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2113G>T
  hgvsp: ENSP00000442010.1:p.Ala705Ser
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3643G>T
  hgvsp: ENSP00000383274.1:p.Ala1215Ser
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2455G>T
  hgvsp: ENSP00000444693.1:p.Ala819Ser
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2803G>T
  hgvsp: ENSP00000364071.3:p.Ala935Ser
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3643G>T
  hgvsp: ENSP00000264211.7:p.Ala1215Ser
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46747
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1681
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1465
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala1221Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

1-21175985-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175985
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175985
    reference: chr 1
allele count: 1
allele frequency: 8.275405494869249e-6
allele num: 120840
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2803G>C
  hgvsp: ENSP00000364071.3:p.Ala935Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3643G>C
  hgvsp: ENSP00000264211.7:p.Ala1215Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2113G>C
  hgvsp: ENSP00000442010.1:p.Ala705Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3661G>C
  hgvsp: ENSP00000364073.3:p.Ala1221Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2455G>C
  hgvsp: ENSP00000444693.1:p.Ala819Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3661G>C
  hgvsp: ENSP00000473510.1:p.Ala1221Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3643G>C
  hgvsp: ENSP00000383274.1:p.Ala1215Pro
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1681
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala1221Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

1-21175993-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175993
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175993
    reference: chr 1
allele count: 9
allele frequency: 7.455515424633023e-5
allele num: 120716
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2105A>G
  hgvsp: ENSP00000442010.1:p.His702Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3653A>G
  hgvsp: ENSP00000473510.1:p.His1218Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2795A>G
  hgvsp: ENSP00000364071.3:p.His932Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2447A>G
  hgvsp: ENSP00000444693.1:p.His816Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3653A>G
  hgvsp: ENSP00000364073.3:p.His1218Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3635A>G
  hgvsp: ENSP00000383274.1:p.His1212Arg
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3635A>G
  hgvsp: ENSP00000264211.7:p.His1212Arg
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16871
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1680
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 9.25e1
  variant carriers: 0
hgvs: p.His1218Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

1-21175993-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21175993
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21175993
    reference: chr 1
allele count: 1
allele frequency: 8.283906027370025e-6
allele num: 120716
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3653A>C
  hgvsp: ENSP00000364073.3:p.His1218Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2795A>C
  hgvsp: ENSP00000364071.3:p.His932Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3635A>C
  hgvsp: ENSP00000383274.1:p.His1212Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2105A>C
  hgvsp: ENSP00000442010.1:p.His702Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2447A>C
  hgvsp: ENSP00000444693.1:p.His816Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3635A>C
  hgvsp: ENSP00000264211.7:p.His1212Pro
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3653A>C
  hgvsp: ENSP00000473510.1:p.His1218Pro
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46545
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7004
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His1218Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP

1-21176005-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176005
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176005
    reference: chr 1
allele count: 1
allele frequency: 8.304682179812978e-6
allele num: 120414
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2093C>G
  hgvsp: ENSP00000442010.1:p.Ala698Gly
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3623C>G
  hgvsp: ENSP00000383274.1:p.Ala1208Gly
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2435C>G
  hgvsp: ENSP00000444693.1:p.Ala812Gly
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3641C>G
  hgvsp: ENSP00000364073.3:p.Ala1214Gly
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2783C>G
  hgvsp: ENSP00000364071.3:p.Ala928Gly
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3641C>G
  hgvsp: ENSP00000473510.1:p.Ala1214Gly
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3623C>G
  hgvsp: ENSP00000264211.7:p.Ala1208Gly
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6925
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45897
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala1214Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

1-21176016-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176016
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176016
    reference: chr 1
allele count: 38
allele frequency: 3.171423802370222e-4
allele num: 119820
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2772A>G
  hgvsp: ENST00000374935.3:c.2772A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3612A>G
  hgvsp: ENST00000264211.8:c.3612A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3630A>G
  hgvsp: ENST00000602326.1:c.3630A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3612A>G
  hgvsp: ENST00000400422.1:c.3612A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2424A>G
  hgvsp: ENST00000536266.1:c.2424A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2082A>G
  hgvsp: ENST00000537738.1:c.2082A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3630A>G
  hgvsp: ENST00000374937.3:c.3630A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7632
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16650
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27836
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1432
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44473
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro1210Pro
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

1-21176032-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176032
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176032
    reference: chr 1
allele count: 1
allele frequency: 8.599339570720968e-6
allele num: 116288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-9C>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-9C>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-9C>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-9C>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-9C>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-9C>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-9C>T
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15103
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5923
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1915
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1243
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

1-21176035-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176035
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176036
    reference: chr 1
allele count: 11
allele frequency: 9.668459726470485e-5
allele num: 113772
alternate allele: GC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-13dupG
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-13dupG
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-13dupG
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-13dupG
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-13dupG
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-13dupG
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-13dupG
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7299
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16141
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9208
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13395
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2245
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2711
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

1-21176035-GCCCCC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176035
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176030
    reference: chr 1
allele count: 1
allele frequency: 8.789508842245894e-6
allele num: 113772
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-17_2417-13delGGGGG
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-17_2765-13delGGGGG
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-17_3623-13delGGGGG
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-17_2075-13delGGGGG
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-17_3605-13delGGGGG
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-17_3623-13delGGGGG
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-17_3605-13delGGGGG
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7299
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27713
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: GCCCCC
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP

1-21176036-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176036
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176036
    reference: chr 1
allele count: 9
allele frequency: 7.966434754899357e-5
allele num: 112974
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-13G>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-13G>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-13G>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-13G>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-13G>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-13G>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-13G>C
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12746
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7502
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14443
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9868
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1913
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14087
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/1-21176036-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176036
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176036
    reference: chr 1
allele count: 6
allele frequency: 5.310956503266238e-5
allele num: 112974
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-13G>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-13G>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-13G>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-13G>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-13G>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-13G>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-13G>T
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7502
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14443
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9868
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12746
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2603
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14087
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26392
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1007
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

1-21176036-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176036
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176036
    reference: chr 1
allele count: 1
allele frequency: 8.851594172110397e-6
allele num: 112974
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-13G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-13G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-13G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-13G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-13G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-13G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-13G>A
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7502
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9868
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1913
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1417
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

1-21176041-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176041
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176041
    reference: chr 1
allele count: 1
allele frequency: 9.328184175668365e-6
allele num: 107202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-18G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-18G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-18G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-18G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-18G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-18G>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-18G>A
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3832
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20446
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2684
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3341
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-21176041-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176041
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176040
    reference: chr 1
allele count: 1
allele frequency: 9.328184175668365e-6
allele num: 107202
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-19delT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-19delT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-19delT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-19delT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-19delT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-19delT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-19delT
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5384
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15605
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9970
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3341
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20446
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1347
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: CA
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/1-21176042-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176042
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176042
    reference: chr 1
allele count: 5472
allele frequency: 5.405191828993638e-2
allele num: 101236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-19T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-19T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-19T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-19T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-19T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-19T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-19T>G
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6858
  bin: 2.75e1
  variant carriers: 1057
genotype depth: GenotypeDepth
  all individuals: 6770
  bin: 2.25e1
  variant carriers: 1160
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.25e1
  variant carriers: 157
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 5.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 3.25e1
  variant carriers: 654
genotype depth: GenotypeDepth
  all individuals: 19781
  bin: 1.25e1
  variant carriers: 488
genotype depth: GenotypeDepth
  all individuals: 8546
  bin: 1.75e1
  variant carriers: 1006
genotype depth: GenotypeDepth
  all individuals: 6987
  bin: 7.5e0
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 3.75e1
  variant carriers: 371
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 4348
  bin: 2.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 4.25e1
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 6243
  bin: 9.75e1
  variant carriers: 4652
genotype quality: GenotypeQuality
  all individuals: 2877
  bin: 7.5e0
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 8.25e1
  variant carriers: 56
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 1.25e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 2610
  bin: 6.75e1
  variant carriers: 59
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 5.25e1
  variant carriers: 57
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 8.75e1
  variant carriers: 58
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 3.75e1
  variant carriers: 38
num of homozygotes: 211
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

1-21176042-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176042
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176042
    reference: chr 1
allele count: 1
allele frequency: 9.877909044213521e-6
allele num: 101236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-19T>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-19T>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-19T>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-19T>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-19T>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-19T>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-19T>C
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6858
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6987
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9606
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3786
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

1-21176043-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176043
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176043
    reference: chr 1
allele count: 1
allele frequency: 9.998800143982723e-6
allele num: 100012
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-20T>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-20T>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-20T>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-20T>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-20T>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-20T>A
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-20T>A
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4478
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10683
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26966
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4786
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3042
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

1-21176043-AAAAAAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176043
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176037
    reference: chr 1
allele count: 1
allele frequency: 9.998800143982723e-6
allele num: 100012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-26_2765-21delCTTTTT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-26_3623-21delCTTTTT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-26_2417-21delCTTTTT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-26_3605-21delCTTTTT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-26_2075-21delCTTTTT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-26_3623-21delCTTTTT
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-26_3605-21delCTTTTT
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1354
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3042
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2905
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4786
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: AAAAAAG
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD

1-21176044-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176044
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176044
    reference: chr 1
allele count: 1
allele frequency: 9.944114078876713e-6
allele num: 100562
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-21T>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-21T>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-21T>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-21T>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-21T>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-21T>C
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-21T>C
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8077
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7717
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4812
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11068
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3015
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-21176045-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176045
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176045
    reference: chr 1
allele count: 1
allele frequency: 9.942729875914731e-6
allele num: 100576
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-22T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-22T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-22T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-22T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-22T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-22T>G
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-22T>G
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5825
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8066
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21551
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2936
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1338
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-21176050-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21176050
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 21176050
    reference: chr 1
allele count: 3
allele frequency: 3.799007192786952e-5
allele num: 78968
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000444693
  ensembl transcript: ENST00000536266
  gene symbol: EIF4G3
  hgvsc: ENST00000536266.1:c.2417-27A>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000473510
  ensembl transcript: ENST00000602326
  gene symbol: EIF4G3
  hgvsc: ENST00000602326.1:c.3623-27A>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000442010
  ensembl transcript: ENST00000537738
  gene symbol: EIF4G3
  hgvsc: ENST00000537738.1:c.2075-27A>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000383274
  ensembl transcript: ENST00000400422
  gene symbol: EIF4G3
  hgvsc: ENST00000400422.1:c.3605-27A>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364073
  ensembl transcript: ENST00000374937
  gene symbol: EIF4G3
  hgvsc: ENST00000374937.3:c.3623-27A>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000264211
  ensembl transcript: ENST00000264211
  gene symbol: EIF4G3
  hgvsc: ENST00000264211.8:c.3605-27A>T
  variant of: http://identifiers.org/hgnc/3298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075151
  ensembl protein: ENSP00000364071
  ensembl transcript: ENST00000374935
  gene symbol: EIF4G3
  hgvsc: ENST00000374935.3:c.2765-27A>T
  variant of: http://identifiers.org/hgnc/3298
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7275
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6512
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 2905
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3261
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2218
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38134
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5964
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3313
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2998
bin: 7.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 8.05e-1

DP
type: SiteQuality
SIO_000300: 2.654913e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.91e-1

QD
type: SiteQuality
SIO_000300: 2.203e1

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.385e0

MQRankSum
type: SiteQuality
SIO_000300: 3.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.092e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.649999999999999e-1

GenotypeQuality
all individuals: 3316
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3263
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5944
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1883
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2907
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38153
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.655988e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.81e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.21e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

QD
type: SiteQuality
SIO_000300: 1.353e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.487e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 7.445e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.296e0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 2

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

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

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

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

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

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

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

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 20

GenotypeQuality
all individuals: 20
bin: 8.25e1
variant carriers: 13

GenotypeQuality
all individuals: 60487
bin: 9.75e1
variant carriers: 60460

GenotypeQuality
all individuals: 26
bin: 6.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 10

African
type: Population
allele count: 8480
allele frequency: 8.149144724197578e-1
allele num: 10406
num of homozygotes: 3447

South Asian
type: Population
allele count: 16510
allele frequency: 9.998788759689923e-1
allele num: 16512
num of homozygotes: 8254

European (Finnish)
type: Population
allele count: 6614
allele frequency: 1.0e0
allele num: 6614
num of homozygotes: 3307

European (Non-Finnish)
type: Population
allele count: 66723
allele frequency: 9.99745280191789e-1
allele num: 66740
num of homozygotes: 33353

Latino
type: Population
allele count: 11479
allele frequency: 9.914493003973053e-1
allele num: 11578
num of homozygotes: 5691

East Asian
type: Population
allele count: 8654
allele frequency: 1.0e0
allele num: 8654
num of homozygotes: 4327

Other
type: Population
allele count: 903
allele frequency: 9.944933920704846e-1
allele num: 908
num of homozygotes: 449

DP
type: SiteQuality
SIO_000300: 6.426688e6

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 3.082e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.538e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4252
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31517
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9829
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2892
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6179
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1215
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 1.953e0

VQSLOD
type: SiteQuality
SIO_000300: -6.439e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.45e0

DP
type: SiteQuality
SIO_000300: 2.025741e6

QD
type: SiteQuality
SIO_000300: 2.605e1

GenotypeQuality
all individuals: 1753
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2891
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3051
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4251
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9829
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31523
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
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: 908
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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.437e0

DP
type: SiteQuality
SIO_000300: 2.024889e6

QD
type: SiteQuality
SIO_000300: 1.309e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -6.28e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1753
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6160
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31527
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3052
bin: 7.25e1
variant carriers: 0

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

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

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

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: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.362e1

FS
type: SiteQuality
SIO_000300: 7.731e0

DP
type: SiteQuality
SIO_000300: 2.024775e6

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.141e0

VQSLOD
type: SiteQuality
SIO_000300: 6.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.899e0

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

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

GenotypeQuality
all individuals: 3053
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6156
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1754
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9829
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4252
bin: 7.75e1
variant carriers: 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: 10406
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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.492208103572285e-5
allele num: 66736
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: -1.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.38e-1

FS
type: SiteQuality
SIO_000300: 1.103e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.293e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.1e-1

DP
type: SiteQuality
SIO_000300: 2.024461e6

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

GenotypeQuality
all individuals: 6140
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9828
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31545
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1753
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3049
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
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

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

FS
type: SiteQuality
SIO_000300: 8.858000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.748e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.05e-1

QD
type: SiteQuality
SIO_000300: 9.789999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.922e0

DP
type: SiteQuality
SIO_000300: 2.0235e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4248
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6139
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1216
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3051
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

European (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
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

ReadPosRankSum
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SIO_000300: 2.22e-1

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

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

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

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

Other
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allele frequency: 0.0e0
allele num: 908
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

FS
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BaseQRankSum
type: SiteQuality
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MQ
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 3.0e-4

DP
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QD
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ClippingRankSum
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SIO_000300: 8.400000000000001e-2

MQRankSum
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VQSLOD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

East Asian
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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: 906
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

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

FS
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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MQ
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.991e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e-1

MQRankSum
type: SiteQuality
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ReadPosRankSum
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

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: 7.25e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16506
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: 906
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.421e1

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.832e0

MQRankSum
type: SiteQuality
SIO_000300: -1.205e0

ReadPosRankSum
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SIO_000300: -1.264e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.86e0

DP
type: SiteQuality
SIO_000300: 2.019881e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.16e-1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.801e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.737e0

ReadPosRankSum
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SIO_000300: -1.044e0

DP
type: SiteQuality
SIO_000300: 2.01967e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 906
num of homozygotes: 0

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

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

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

East Asian
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allele frequency: 0.0e0
allele num: 8652
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

South Asian
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allele frequency: 0.0e0
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DP
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MQRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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QD
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MQ
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SIO_000300: 6.0e1

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

East Asian
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allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 3.000120004800192e-5
allele num: 66664
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

African
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East Asian
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MQ
type: SiteQuality
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ClippingRankSum
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DP
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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GenotypeQuality
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variant carriers: 1

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

Other
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num of homozygotes: 0

African
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South Asian
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num of homozygotes: 0

FS
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -1.205e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.305e0

MQRankSum
type: SiteQuality
SIO_000300: -1.01e-1

DP
type: SiteQuality
SIO_000300: 2.015871e6

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2815
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 548
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31207
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9559
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4149
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502178158329578e-5
allele num: 66570
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

DP
type: SiteQuality
SIO_000300: 2.001997e6

QD
type: SiteQuality
SIO_000300: 9.890000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.125e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.45e-1

MQ
type: SiteQuality
SIO_000300: 5.89e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.32e0

FS
type: SiteQuality
SIO_000300: 4.824e0

GenotypeQuality
all individuals: 408
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9280
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1691
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2881
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29946
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503940323647958e-5
allele num: 66492
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 9.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.08e-1

QD
type: SiteQuality
SIO_000300: 8.08e0

FS
type: SiteQuality
SIO_000300: 4.135e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.974898e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.382e0

GenotypeQuality
all individuals: 1574
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3104
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3008
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3737
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21249
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2548
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5992
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 1
allele frequency: 6.181233774261343e-5
allele num: 16178
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10138
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66304
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.84947e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

QD
type: SiteQuality
SIO_000300: 1.094e1

VQSLOD
type: SiteQuality
SIO_000300: -2.315e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.27e-1

GenotypeQuality
all individuals: 2462
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2739
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3517
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1726
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7248
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3856
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1109
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1626
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 6450
bin: 9.75e1
variant carriers: 561

South Asian
type: Population
allele count: 253
allele frequency: 1.566951566951567e-2
allele num: 16146
num of homozygotes: 4

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.516530178950561e-4
allele num: 6594
num of homozygotes: 0

East Asian
type: Population
allele count: 174
allele frequency: 2.030812324929972e-2
allele num: 8568
num of homozygotes: 5

Latino
type: Population
allele count: 3
allele frequency: 2.612330198537095e-4
allele num: 11484
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.464285714285714e-3
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 73
allele frequency: 7.212013436079827e-3
allele num: 10122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 74
allele frequency: 1.117554669566268e-3
allele num: 66216
num of homozygotes: 1

VQSLOD
type: SiteQuality
SIO_000300: 5.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.547e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.23e-1

DP
type: SiteQuality
SIO_000300: 1.82672e6

QD
type: SiteQuality
SIO_000300: 1.355e1

GenotypeQuality
all individuals: 358
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2043
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1660
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3517
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1626
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1109
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6450
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2462
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1726
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3634
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510209012927389e-5
allele num: 66216
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.82672e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.49e0

QD
type: SiteQuality
SIO_000300: 1.355e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.547e0

GenotypeQuality
all individuals: 654
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 541
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variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 1183
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
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variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 338
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1750
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1254
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.244e0

QD
type: SiteQuality
SIO_000300: 1.448e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

DP
type: SiteQuality
SIO_000300: 4.87884e5

BaseQRankSum
type: SiteQuality
SIO_000300: -4.03e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.875e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.71e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.95e-1

GenotypeQuality
all individuals: 838
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1600
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 536
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3741
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 54
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 397
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1260
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 2.032520325203252e-3
allele num: 492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1762
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

QD
type: SiteQuality
SIO_000300: 9.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.35e0

DP
type: SiteQuality
SIO_000300: 4.90511e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.39e-2

FS
type: SiteQuality
SIO_000300: 3.739e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.414e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

GenotypeQuality
all individuals: 536
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522533495736906e-4
allele num: 6568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1748
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.86e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.88836e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.35e0

VQSLOD
type: SiteQuality
SIO_000300: -6.552e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.88e-1

QD
type: SiteQuality
SIO_000300: 1.282e1

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

GenotypeQuality
all individuals: 637
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 349
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3738
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1307
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.304461257500652e-4
allele num: 7666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1732
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.808e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.97e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.313e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

QD
type: SiteQuality
SIO_000300: 1.011e1

DP
type: SiteQuality
SIO_000300: 4.85867e5

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-3

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 636
bin: 8.25e1
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GenotypeQuality
all individuals: 757
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.040816326530612e-3
allele num: 490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7664
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

DP
type: SiteQuality
SIO_000300: 4.82636e5

MQ
type: SiteQuality
SIO_000300: 5.934e1

QD
type: SiteQuality
SIO_000300: 1.06e1

VQSLOD
type: SiteQuality
SIO_000300: 2.88e-1

GenotypeQuality
all individuals: 690
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2824
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1551
bin: 1.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9024
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8728
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.202212070209185e-4
allele num: 8318
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5950
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.11e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

VQSLOD
type: SiteQuality
SIO_000300: -3.406e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.45e-1

DP
type: SiteQuality
SIO_000300: 9.95145e5

QD
type: SiteQuality
SIO_000300: 1.607e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 2823
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1704
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.138433515482696e-4
allele num: 8784
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9050
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47968
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5976
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.134e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.031e0

DP
type: SiteQuality
SIO_000300: 1.003286e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

GenotypeQuality
all individuals: 1621
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7613
bin: 3.25e1
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 2338
bin: 4.75e1
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GenotypeQuality
all individuals: 2896
bin: 9.75e1
variant carriers: 67

GenotypeQuality
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GenotypeQuality
all individuals: 786
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variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.669449081803005e-4
allele num: 5990
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

South Asian
type: Population
allele count: 64
allele frequency: 7.081212657667626e-3
allele num: 9038
num of homozygotes: 3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.050188617352796e-5
allele num: 48776
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.996e1

QD
type: SiteQuality
SIO_000300: 1.302e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.295e0

DP
type: SiteQuality
SIO_000300: 1.05118e6

VQSLOD
type: SiteQuality
SIO_000300: 2.57e0

GenotypeQuality
all individuals: 2884
bin: 9.75e1
variant carriers: 45

GenotypeQuality
all individuals: 446
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6682
bin: 3.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 14088
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14545
bin: 2.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6016
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.087665869045029e-4
allele num: 9194
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 7.704160246533128e-4
allele num: 9086
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.182592242194891e-3
allele num: 8456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.646364302581223e-4
allele num: 49124
num of homozygotes: 0

East Asian
type: Population
allele count: 14
allele frequency: 2.118003025718608e-3
allele num: 6610
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.436781609195402e-3
allele num: 696
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e-1

DP
type: SiteQuality
SIO_000300: 1.111265e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.209e0

QD
type: SiteQuality
SIO_000300: 1.192e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

MQ
type: SiteQuality
SIO_000300: 5.866e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

GenotypeQuality
all individuals: 534
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2884
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 787
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variant carriers: 0

GenotypeQuality
all individuals: 1403
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GenotypeQuality
all individuals: 1375
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GenotypeQuality
all individuals: 4927
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variant carriers: 0

GenotypeQuality
all individuals: 6682
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14545
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
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variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.087665869045029e-4
allele num: 9194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.106994544418207e-5
allele num: 49124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.182592242194891e-4
allele num: 8456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9086
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6016
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.866e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.209e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.192e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

DP
type: SiteQuality
SIO_000300: 1.111265e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e-1

GenotypeQuality
all individuals: 784
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
all individuals: 3106
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GenotypeQuality
all individuals: 363
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variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6980
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10028
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.310615989515072e-3
allele num: 6104
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8800
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52306
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e-1

QD
type: SiteQuality
SIO_000300: 7.85e0

MQRankSum
type: SiteQuality
SIO_000300: -6.54e-1

MQ
type: SiteQuality
SIO_000300: 5.827e1

DP
type: SiteQuality
SIO_000300: 1.208566e6

GenotypeQuality
all individuals: 3118
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1202
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 354
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GenotypeQuality
all individuals: 3041
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6972
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.138433515482696e-4
allele num: 8784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52226
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9990
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.523e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

QD
type: SiteQuality
SIO_000300: 9.18e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.229695e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

GenotypeQuality
all individuals: 738
bin: 5.75e1
variant carriers: 25

GenotypeQuality
all individuals: 1386
bin: 4.75e1
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GenotypeQuality
all individuals: 3316
bin: 7.5e0
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GenotypeQuality
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bin: 3.25e1
variant carriers: 79

GenotypeQuality
all individuals: 2934
bin: 1.25e1
variant carriers: 69

GenotypeQuality
all individuals: 1069
bin: 6.75e1
variant carriers: 16

GenotypeQuality
all individuals: 361
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GenotypeQuality
all individuals: 6629
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variant carriers: 15

GenotypeQuality
all individuals: 121
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GenotypeQuality
all individuals: 173
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 46
allele frequency: 9.56738768718802e-3
allele num: 4808
num of homozygotes: 0

Other
type: Population
allele count: 7
allele frequency: 1.590909090909091e-2
allele num: 440
num of homozygotes: 0

East Asian
type: Population
allele count: 32
allele frequency: 8.303061754021795e-3
allele num: 3854
num of homozygotes: 0

African
type: Population
allele count: 34
allele frequency: 6.186317321688501e-3
allele num: 5496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 226
allele frequency: 7.606866374957927e-3
allele num: 29710
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 1.182592242194891e-3
allele num: 4228
num of homozygotes: 0

South Asian
type: Population
allele count: 153
allele frequency: 3.103448275862069e-2
allele num: 4930
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.513078e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.28e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.958e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

QD
type: SiteQuality
SIO_000300: 1.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4808
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3854
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.513078e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.958e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

QD
type: SiteQuality
SIO_000300: 1.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2414
bin: 3.75e1
variant carriers: 250

GenotypeQuality
all individuals: 7029
bin: 2.25e1
variant carriers: 359

GenotypeQuality
all individuals: 173
bin: 9.25e1
variant carriers: 29

GenotypeQuality
all individuals: 380
bin: 7.25e1
variant carriers: 55

GenotypeQuality
all individuals: 3267
bin: 3.25e1
variant carriers: 235

GenotypeQuality
all individuals: 121
bin: 8.75e1
variant carriers: 20

GenotypeQuality
all individuals: 361
bin: 7.75e1
variant carriers: 43

GenotypeQuality
all individuals: 1069
bin: 6.75e1
variant carriers: 54

GenotypeQuality
all individuals: 738
bin: 5.75e1
variant carriers: 91

GenotypeQuality
all individuals: 6629
bin: 6.25e1
variant carriers: 65

European (Finnish)
type: Population
allele count: 80
allele frequency: 1.892147587511826e-2
allele num: 4228
num of homozygotes: 0

Latino
type: Population
allele count: 214
allele frequency: 4.450915141430949e-2
allele num: 4808
num of homozygotes: 1

East Asian
type: Population
allele count: 173
allele frequency: 4.488842760768033e-2
allele num: 3854
num of homozygotes: 0

African
type: Population
allele count: 427
allele frequency: 7.769286754002912e-2
allele num: 5496
num of homozygotes: 5

Other
type: Population
allele count: 23
allele frequency: 5.227272727272727e-2
allele num: 440
num of homozygotes: 0

South Asian
type: Population
allele count: 219
allele frequency: 4.442190669371197e-2
allele num: 4930
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1384
allele frequency: 4.658364187142376e-2
allele num: 29710
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.958e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

DP
type: SiteQuality
SIO_000300: 1.513078e6

GenotypeQuality
all individuals: 2414
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7029
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3316
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1234
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1611
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3267
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 121
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3854
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4808
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4228
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.028397565922921e-4
allele num: 4930
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.365870077415012e-5
allele num: 29710
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.819505094614265e-4
allele num: 5496
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.958e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 1.513078e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4808
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.365870077415012e-5
allele num: 29710
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4930
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.958e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

QD
type: SiteQuality
SIO_000300: 1.62e0

MQRankSum
type: SiteQuality
SIO_000300: 2.28e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.513078e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

GenotypeQuality
all individuals: 330
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7881
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2561
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2167
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 623
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1187
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3435
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 2.039983680130559e-4
allele num: 4902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.716443529007896e-4
allele num: 29130
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4748
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3838
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 7.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

MQ
type: SiteQuality
SIO_000300: 6.065e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.311e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 1.281333e6

FS
type: SiteQuality
SIO_000300: 1.862e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

GenotypeQuality
all individuals: 3117
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2167
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1372
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7881
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7142
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 9.75e1
variant carriers: 37

GenotypeQuality
all individuals: 1187
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.039983680130559e-4
allele num: 4902
num of homozygotes: 0

African
type: Population
allele count: 24
allele frequency: 4.854368932038835e-3
allele num: 4944
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3838
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4748
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 5.835907998626845e-4
allele num: 29130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4414
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 1.862e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.311e-1

QD
type: SiteQuality
SIO_000300: 7.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

DP
type: SiteQuality
SIO_000300: 1.281333e6

MQ
type: SiteQuality
SIO_000300: 6.065e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
all individuals: 128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3862
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2167
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3435
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
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variant carriers: 0

GenotypeQuality
all individuals: 1228
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7142
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4944
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4748
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4414
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.432887058015791e-5
allele num: 29130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4902
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.065e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.311e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 1.281333e6

FS
type: SiteQuality
SIO_000300: 1.862e0

QD
type: SiteQuality
SIO_000300: 7.43e0

GenotypeQuality
all individuals: 2155
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8340
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1519
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 544
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2854
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 5.639097744360903e-4
allele num: 5320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.537515375153752e-4
allele num: 6504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5022
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.497253021676156e-5
allele num: 40044
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.89e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.37e-1

QD
type: SiteQuality
SIO_000300: 1.218e1

DP
type: SiteQuality
SIO_000300: 1.503716e6

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

GenotypeQuality
all individuals: 43425
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 7.5e0
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GenotypeQuality
all individuals: 311
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6821
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65446
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.733624454148471e-5
allele num: 11450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15116
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.756e0

FS
type: SiteQuality
SIO_000300: 4.227e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

DP
type: SiteQuality
SIO_000300: 1.621204e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e0

VQSLOD
type: SiteQuality
SIO_000300: -1.063e0

MQRankSum
type: SiteQuality
SIO_000300: 7.73e-1

QD
type: SiteQuality
SIO_000300: 1.114e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.92e0

GenotypeQuality
all individuals: 44393
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.5e0
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GenotypeQuality
all individuals: 272
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1457
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 259
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.307702366941284e-4
allele num: 15294
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65668
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.069e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.757e0

VQSLOD
type: SiteQuality
SIO_000300: -2.779e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-1

DP
type: SiteQuality
SIO_000300: 1.62925e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.885e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 4.606e0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 2.25e1
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GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1923
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variant carriers: 1

GenotypeQuality
all individuals: 1475
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variant carriers: 0

GenotypeQuality
all individuals: 46311
bin: 6.25e1
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GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.223549912870301e-5
allele num: 16068
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66304
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.654855e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 1.248e1

FS
type: SiteQuality
SIO_000300: 8.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.66e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
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GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.75e1
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GenotypeQuality
all individuals: 1472
bin: 7.75e1
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GenotypeQuality
all individuals: 703
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variant carriers: 0

GenotypeQuality
all individuals: 1924
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
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: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505026789476853e-5
allele num: 66444
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

DP
type: SiteQuality
SIO_000300: 1.659003e6

VQSLOD
type: SiteQuality
SIO_000300: -1.821e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.5331e1

QD
type: SiteQuality
SIO_000300: 2.885e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.77e-1

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 390
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46621
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1691
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1924
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66458
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.170554115759595e-5
allele num: 16206
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.07e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.792e0

DP
type: SiteQuality
SIO_000300: 1.659352e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.411e0

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7023
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46614
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.65508109897385e-4
allele num: 66462
num of homozygotes: 0

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

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

African
type: Population
allele count: 2
allele frequency: 1.92789666473877e-4
allele num: 10374
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.251e1

DP
type: SiteQuality
SIO_000300: 1.660151e6

FS
type: SiteQuality
SIO_000300: 5.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

GenotypeQuality
all individuals: 1461
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46760
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1686
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7037
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66540
num of homozygotes: 0

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

South Asian
type: Population
allele count: 17
allele frequency: 1.044739429695182e-3
allele num: 16272
num of homozygotes: 1

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.056e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.2e0

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

DP
type: SiteQuality
SIO_000300: 1.663228e6

FS
type: SiteQuality
SIO_000300: 5.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.665e0

GenotypeQuality
all individuals: 1686
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 696
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7037
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1950
bin: 9.75e1
variant carriers: 13

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.803426510369702e-4
allele num: 66540
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

DP
type: SiteQuality
SIO_000300: 1.663228e6

FS
type: SiteQuality
SIO_000300: 5.23e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.056e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.665e0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7031
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.2306177701206e-4
allele num: 16252
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
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: -2.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.46e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

QD
type: SiteQuality
SIO_000300: 1.121e1

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.64e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.317e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.662525e6

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

GenotypeQuality
all individuals: 1465
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46747
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7031
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 340
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503036132988637e-5
allele num: 66532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16252
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -6.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.662525e6

MQRankSum
type: SiteQuality
SIO_000300: -2.57e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.64e-1

QD
type: SiteQuality
SIO_000300: 1.121e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.317e0

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

GenotypeQuality
all individuals: 1462
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46545
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7004
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66480
num of homozygotes: 0

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

South Asian
type: Population
allele count: 9
allele frequency: 5.55212831585441e-4
allele num: 16210
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.96e0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.13e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.536e0

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

DP
type: SiteQuality
SIO_000300: 1.660957e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1680
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1462
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 9.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.66183574879227e-5
allele num: 10350
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16210
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

QD
type: SiteQuality
SIO_000300: 1.13e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

FS
type: SiteQuality
SIO_000300: 2.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.536e0

DP
type: SiteQuality
SIO_000300: 1.660957e6

GenotypeQuality
all individuals: 1454
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1673
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1922
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66396
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.669309611293753e-5
allele num: 10342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16026
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.7e-2

DP
type: SiteQuality
SIO_000300: 1.654054e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQRankSum
type: SiteQuality
SIO_000300: 7.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.006e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.337e1

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1951
bin: 9.75e1
variant carriers: 38

GenotypeQuality
all individuals: 2036
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1649
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6843
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 293
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 37
allele frequency: 3.589445091191308e-3
allele num: 10308
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66124
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.338742393509128e-5
allele num: 15776
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.33e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.55e-1

DP
type: SiteQuality
SIO_000300: 1.640348e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.484e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 7.42e-1

QD
type: SiteQuality
SIO_000300: 1.166e1

VQSLOD
type: SiteQuality
SIO_000300: 3.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e-1

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

GenotypeQuality
all individuals: 252
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8526
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34939
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1384
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1574
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11314
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9944
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.711409395973154e-5
allele num: 14900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64222
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.699e0

VQSLOD
type: SiteQuality
SIO_000300: 9.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

DP
type: SiteQuality
SIO_000300: 1.548731e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-2

QD
type: SiteQuality
SIO_000300: 1.148e1

GenotypeQuality
all individuals: 85
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 12480
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27713
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 5664
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1820
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1332
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.046663937781416e-4
allele num: 9772
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8344
num of homozygotes: 0

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

South Asian
type: Population
allele count: 7
allele frequency: 4.868549172346641e-4
allele num: 14378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11142
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.185220576524925e-5
allele num: 62790
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.17e0

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

DP
type: SiteQuality
SIO_000300: 1.47802e6

GenotypeQuality
all individuals: 12480
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1820
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5664
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1332
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2245
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2711
bin: 9.75e1
variant carriers: 1

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11142
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8344
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14378
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.023331968890708e-4
allele num: 9772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62790
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

QD
type: SiteQuality
SIO_000300: 1.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

DP
type: SiteQuality
SIO_000300: 1.47802e6

GenotypeQuality
all individuals: 1312
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2603
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1007
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5560
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26392
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.445504481063891e-4
allele num: 62262
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11092
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

DP
type: SiteQuality
SIO_000300: 1.485823e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.14e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

GenotypeQuality
all individuals: 5560
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1913
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 629
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1417
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11092
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62262
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 4.202857943401513e-4
allele num: 14276
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.348e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

DP
type: SiteQuality
SIO_000300: 1.485823e6

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.14e-1

GenotypeQuality
all individuals: 26392
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14087
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5560
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1007
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2603
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.029018316526034e-4
allele num: 9718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11092
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14276
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.14e-1

DP
type: SiteQuality
SIO_000300: 1.485823e6

VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

QD
type: SiteQuality
SIO_000300: 1.348e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

GenotypeQuality
all individuals: 283
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15740
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4777
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.083658430862592e-4
allele num: 9228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7994
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13446
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6278
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58796
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

DP
type: SiteQuality
SIO_000300: 1.326803e6

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 7.125e0

QD
type: SiteQuality
SIO_000300: 7.39e0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

GenotypeQuality
all individuals: 485
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15740
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3832
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2684
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1561
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4777
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.391435011269723e-5
allele num: 10648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58796
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13446
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7994
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9228
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

QD
type: SiteQuality
SIO_000300: 7.39e0

FS
type: SiteQuality
SIO_000300: 7.125e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

DP
type: SiteQuality
SIO_000300: 1.326803e6

GenotypeQuality
all individuals: 3786
bin: 3.25e1
variant carriers: 29

GenotypeQuality
all individuals: 24322
bin: 2.25e1
variant carriers: 21

GenotypeQuality
all individuals: 9606
bin: 6.25e1
variant carriers: 47

GenotypeQuality
all individuals: 586
bin: 1.75e1
variant carriers: 13

GenotypeQuality
all individuals: 673
bin: 7.75e1
variant carriers: 58

GenotypeQuality
all individuals: 297
bin: 2.5e0
variant carriers: 7

GenotypeQuality
all individuals: 725
bin: 7.25e1
variant carriers: 48

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 86

GenotypeQuality
all individuals: 866
bin: 5.75e1
variant carriers: 61

GenotypeQuality
all individuals: 225
bin: 4.75e1
variant carriers: 35

Other
type: Population
allele count: 36
allele frequency: 4.545454545454546e-2
allele num: 792
num of homozygotes: 0

African
type: Population
allele count: 232
allele frequency: 2.670349907918969e-2
allele num: 8688
num of homozygotes: 4

East Asian
type: Population
allele count: 925
allele frequency: 1.23497997329773e-1
allele num: 7490
num of homozygotes: 60

Latino
type: Population
allele count: 1269
allele frequency: 1.244849911712772e-1
allele num: 10194
num of homozygotes: 65

European (Non-Finnish)
type: Population
allele count: 1410
allele frequency: 2.553145257668489e-2
allele num: 55226
num of homozygotes: 10

European (Finnish)
type: Population
allele count: 262
allele frequency: 4.313467237405334e-2
allele num: 6074
num of homozygotes: 5

South Asian
type: Population
allele count: 1338
allele frequency: 1.047604134043219e-1
allele num: 12772
num of homozygotes: 67

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.08e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 1.208006e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e0

QD
type: SiteQuality
SIO_000300: 9.890000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.379e0

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

GenotypeQuality
all individuals: 1275
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2877
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4348
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24322
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6243
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 673
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2610
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6074
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12772
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.151012891344383e-4
allele num: 8688
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55226
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

QD
type: SiteQuality
SIO_000300: 9.890000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.08e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.379e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 1.208006e6

GenotypeQuality
all individuals: 187
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4159
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 685
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2905
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1354
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9952
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7332
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.820034944670938e-5
allele num: 54944
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6024
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.152e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.087e0

DP
type: SiteQuality
SIO_000300: 1.153913e6

MQ
type: SiteQuality
SIO_000300: 5.94e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.971e0

FS
type: SiteQuality
SIO_000300: 2.587e0

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: -2.192e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.17e-1

GenotypeQuality
all individuals: 749
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26966
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10683
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 582
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1730
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4159
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54944
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12336
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7332
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9952
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.94e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.971e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: -2.192e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.17e-1

DP
type: SiteQuality
SIO_000300: 1.153913e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.087e0

FS
type: SiteQuality
SIO_000300: 2.587e0

QD
type: SiteQuality
SIO_000300: 1.152e1

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4170
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27277
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1342
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1730
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 282
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55250
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6042
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9996
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.35795763172189e-4
allele num: 7364
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8680
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

QD
type: SiteQuality
SIO_000300: 1.138e1

MQRankSum
type: SiteQuality
SIO_000300: 6.27e-1

DP
type: SiteQuality
SIO_000300: 1.149599e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.12e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.02e-1

GenotypeQuality
all individuals: 201
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11338
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4166
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3034
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27324
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4804
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8678
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6040
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.809889234778831e-5
allele num: 55252
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12450
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.148559e6

VQSLOD
type: SiteQuality
SIO_000300: 3.72e-1

QD
type: SiteQuality
SIO_000300: 1.378e1

FS
type: SiteQuality
SIO_000300: 3.245e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0